nih-gov/www.ncbi.nlm.nih.gov/dbvar/variants/nssv15702957

247 lines
27 KiB
XML
Raw Blame History

This file contains invisible Unicode characters

This file contains invisible Unicode characters that are indistinguishable to humans but may be processed differently by a computer. If you think that this is intentional, you can safely ignore this warning. Use the Escape button to reveal them.

<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE html PUBLIC "-//W3C//DTD XHTML 1.0 Transitional//EN" "http://www.w3.org/TR/xhtml1/DTD/xhtml1-transitional.dtd">
<html xmlns="http://www.w3.org/1999/xhtml" xml:lang="en" lang="en">
<head><meta http-equiv="Content-Type" content="text/html; charset=utf-8" />
<!-- AppResources meta begin -->
<meta name="paf-app-resources" content="" />
<!-- AppResources meta end -->
<!-- TemplateResources meta begin -->
<meta name="paf_template" content="StdNCol" />
<!-- TemplateResources meta end -->
<!-- Page meta begin -->
<meta name="description" content="nsv4375018 - dbVar Variant - NCBI" />
<!-- Page meta end -->
<!-- Logger begin -->
<meta xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" name="ncbi_app" content="dbvar" /><meta xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" name="ncbi_pdid" content="VariantPage" />
<!-- Logger end -->
<title>nsv4375018 - dbVar Variant - NCBI</title>
<!-- PageFixtures headcontent begin -->
<meta name="ncbi_app" content="dbvar" />
<!-- PageFixtures headcontent end -->
<!-- AppResources external_resources begin -->
<script type="text/javascript" src="/core/jig/1.15.3/js/jig.min.js"></script>
<!-- AppResources external_resources end -->
<!-- Page headcontent begin -->
<!-- Page headcontent end -->
<!-- PageFixtures resources begin -->
<xi:include xmlns:xi="http://www.w3.org/2001/XInclude" href="http://127.0.0.1/sites/static/header_footer" xpointer="xmlns(x=http://www.w3.org/1999/xhtml) xpointer(//x:link[@rel='stylesheet'])"></xi:include>
<!-- PageFixtures resources end -->
<link rel="shortcut icon" href="//www.ncbi.nlm.nih.gov/favicon.ico" /><meta name="ncbi_phid" content="CE8E6C3C7D20094100000000005F0054.m_5" /><script type="text/javascript"><!--
var ScriptPath = '/portal/';
var objHierarchy = {"name":"PAFAppLayout","type":"Layout","realname":"PAFAppLayout",
"children":[{"name":"PAFAppLayout.AppController","type":"Cluster","realname":"PAFAppLayout.AppController",
"children":[{"name":"PAFAppLayout.AppController.AppResources","type":"Portlet","realname":"PAFAppLayout.AppController.AppResources","shortname":"AppResources"},
{"name":"PAFAppLayout.AppController.RequestProcessor","type":"Portlet","realname":"PAFAppLayout.AppController.RequestProcessor","shortname":"RequestProcessor"},
{"name":"PAFAppLayout.AppController.Controller","type":"Cluster","realname":"PAFAppLayout.AppController.Controller",
"children":[{"name":"PAFAppLayout.AppController.Controller.PAFPassController","type":"Portlet","realname":"PAFAppLayout.AppController.Controller.PAFControllerSelector.PAFPassController","shortname":"PAFPassController"}]},
{"name":"PAFAppLayout.AppController.Page","type":"Cluster","realname":"PAFAppLayout.AppController.Page",
"children":[{"name":"PAFAppLayout.AppController.Page.PAFPageSelectorData","type":"Portlet","realname":"PAFAppLayout.AppController.Page.PAFPageSelector.PAFPageSelectorData","shortname":"PAFPageSelectorData"},
{"name":"PAFAppLayout.AppController.Page.dbVar_VariantPage","type":"Cluster","realname":"PAFAppLayout.AppController.Page.dbVar_VariantPage",
"children":[{"name":"PAFAppLayout.AppController.Page.dbVar_VariantPage.MainPortlet","type":"Portlet","realname":"PAFAppLayout.AppController.Page.dbVar_VariantPage.MainPortlet","shortname":"MainPortlet"},
{"name":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_VariantPage_P","type":"Portlet","realname":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_VariantPage_P","shortname":"dbVar_VariantPage_P"},
{"name":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_VariantPage_Tabs","type":"Portlet","realname":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_VariantPage_Tabs","shortname":"dbVar_VariantPage_Tabs"},
{"name":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_VariantPage_Ideo","type":"Portlet","realname":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_VariantPage_Ideo","shortname":"dbVar_VariantPage_Ideo"},
{"name":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_Variant_FilterP","type":"Portlet","realname":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_Variant_FilterP","shortname":"dbVar_Variant_FilterP"},
{"name":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_Variant_FilterOtherResourcesP","type":"Portlet","realname":"PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_Variant_FilterOtherResourcesP","shortname":"dbVar_Variant_FilterOtherResourcesP"}]}]},
{"name":"PAFAppLayout.AppController.PageFixtures","type":"Cluster","realname":"PAFAppLayout.AppController.PageFixtures",
"children":[{"name":"PAFAppLayout.AppController.PageFixtures.PageFixturesP","type":"Portlet","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.PageFixturesP","shortname":"PageFixturesP"},
{"name":"PAFAppLayout.AppController.PageFixtures.SearchBar","type":"Cluster","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.SearchBar",
"children":[{"name":"PAFAppLayout.AppController.PageFixtures.SearchBar.SearchBarChooser","type":"Portlet","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.SearchBar.SearchBarChooser","shortname":"SearchBarChooser"},
{"name":"PAFAppLayout.AppController.PageFixtures.SearchBar.PAFSearchBar","type":"Portlet","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.SearchBar.PAFSearchBar","shortname":"PAFSearchBar"}]},
{"name":"PAFAppLayout.AppController.PageFixtures.HeaderFooter","type":"Cluster","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.HeaderFooter",
"children":[{"name":"PAFAppLayout.AppController.PageFixtures.HeaderFooter.NCBIBreadcrumbs","type":"Portlet","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.HeaderFooter.NCBIBreadcrumbs","shortname":"NCBIBreadcrumbs"},
{"name":"PAFAppLayout.AppController.PageFixtures.HeaderFooter.NCBIHelpDesk","type":"Portlet","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.HeaderFooter.NCBIHelpDesk","shortname":"NCBIHelpDesk"},
{"name":"PAFAppLayout.AppController.PageFixtures.HeaderFooter.NCBIApplog_NoScript_Ping","type":"Portlet","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.HeaderFooter.NCBIApplog_NoScript_Ping","shortname":"NCBIApplog_NoScript_Ping"}]},
{"name":"PAFAppLayout.AppController.PageFixtures.LocalNavPortlet","type":"Portlet","realname":"PAFAppLayout.AppController.PageFixtures.PAFPageFixtures.LocalNavPortlet","shortname":"LocalNavPortlet"}]},
{"name":"PAFAppLayout.AppController.TemplateResources","type":"Cluster","realname":"PAFAppLayout.AppController.TemplateResources",
"children":[{"name":"PAFAppLayout.AppController.TemplateResources.StdNColResources","type":"Portlet","realname":"PAFAppLayout.AppController.TemplateResources.PAFTemplateResources.StdNColResources","shortname":"StdNColResources"}]},
{"name":"PAFAppLayout.AppController.Logger","type":"Portlet","realname":"PAFAppLayout.AppController.Logger","shortname":"Logger"},
{"name":"PAFAppLayout.AppController.DebugConsole","type":"Portlet","realname":"PAFAppLayout.AppController.DebugConsole","shortname":"DebugConsole"}]}]};
--></script>
<meta name='referrer' content='origin-when-cross-origin'/><link type="text/css" rel="stylesheet" href="//static.pubmed.gov/portal/portal3rc.fcgi/4206115/css/4121862/3974050/3917732/251717/4139921/3428953/14534/45193/4062871/4005757/4054683/3430780/4119132/613474/9685/452438/4059265/4116270.css" /><link type="text/css" rel="stylesheet" href="//static.pubmed.gov/portal/portal3rc.fcgi/4206115/css/3529741/3349418/3529739.css" media="print" /><script type="text/javascript">
var ObjectLinks=[{i:0, ename: "p$ExL", esid:"*", sname: "p$ExL", ssid:"*", dname:"p$el", dsid:"0",m:"CopyValue",p:[],f: function(src, dst) {fn_CopyValue(src, dst);}}]
var ActiveNames = {"p$ExL":1, "PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_Variant_FilterOtherResourcesP.Shutter":0};
</script></head>
<body class="dbvar VariantPage">
<div class="grid">
<div class="col twelve_col nomargin shadow">
<!-- System messages like service outage or JS required; this is handled by the TemplateResources portlet -->
<div class="sysmessages">
<noscript>
<p class="nojs">
<strong>Warning:</strong>
The NCBI web site requires JavaScript to function.
<a href="/guide/browsers/#enablejs" title="Learn how to enable JavaScript" target="_blank">more...</a>
</p>
</noscript>
</div>
<!--/.sysmessage-->
<div class="wrap">
<div class="page">
<div xmlns:xi="http://www.w3.org/2001/XInclude">
<xi:include href="http://127.0.0.1/sites/static/header_footer" xpointer="xmlns(x=http://www.w3.org/1999/xhtml) xpointer(//x:div[@id='universal_header'])"></xi:include>
</div>
<!--/.header-->
<div class="header">
<div class="res_logo"><h1 class="res_name"><a href="/dbvar/" title="dbVar home">dbVar</a></h1><h2 class="res_tagline">Database of genomic structural variation</h2></div>
<div class="search"><form method="get" action="/dbvar/"><div class="search_form"><label for="database" class="offscreen_noflow">Search database</label><select id="database"><optgroup label="Recent"><option value="dbvar" selected="selected">dbVar</option><option value="gap">dbGaP</option><option value="clinvar">ClinVar</option><option value="medgen" class="last">MedGen</option></optgroup><optgroup label="All"><option value="gquery">All Databases</option><option value="assembly">Assembly</option><option value="biocollections">Biocollections</option><option value="bioproject">BioProject</option><option value="biosample">BioSample</option><option value="books">Books</option><option value="clinvar">ClinVar</option><option value="cdd">Conserved Domains</option><option value="gap">dbGaP</option><option value="dbvar">dbVar</option><option value="gene">Gene</option><option value="genome">Genome</option><option value="gds">GEO DataSets</option><option value="geoprofiles">GEO Profiles</option><option value="gtr">GTR</option><option value="ipg">Identical Protein Groups</option><option value="medgen">MedGen</option><option value="mesh">MeSH</option><option value="nlmcatalog">NLM Catalog</option><option value="nuccore">Nucleotide</option><option value="omim">OMIM</option><option value="pmc">PMC</option><option value="protein">Protein</option><option value="proteinclusters">Protein Clusters</option><option value="protfam">Protein Family Models</option><option value="pcassay">PubChem BioAssay</option><option value="pccompound">PubChem Compound</option><option value="pcsubstance">PubChem Substance</option><option value="pubmed">PubMed</option><option value="snp">SNP</option><option value="sra">SRA</option><option value="structure">Structure</option><option value="taxonomy">Taxonomy</option><option value="toolkit">ToolKit</option><option value="toolkitall">ToolKitAll</option><option value="toolkitbookgh">ToolKitBookgh</option></optgroup></select><div class="nowrap"><label for="term" class="offscreen_noflow" accesskey="/">Search term</label><div class="nowrap"><input type="text" name="term" id="term" title="Search dbVar" value="" class="jig-ncbiclearbutton jig-ncbiautocomplete" data-jigconfig="isEnabled:false,disableUrl:'NcbiSearchBarAutoComplCtrl'" autocomplete="off" data-sbconfig="ds:'no',pjs:'no',afs:'yes'" /></div><button id="search" type="submit" class="button_search nowrap" cmd="go">Search</button></div></div><input type="hidden" name="p$a" id="p$a" /><input type="hidden" name="p$l" id="p$l" value="PAFAppLayout" /><input type="hidden" name="p$st" id="p$st" value="dbvar" /><input name="SessionId" id="SessionId" value="CE8B5AF87C7FFCB1_0191SID" disabled="disabled" type="hidden" /><input name="Snapshot" id="Snapshot" value="/projects/dbVar/dbVar@9.7" disabled="disabled" type="hidden" /></form><ul class="inline_list searchlinks"><li>
<a href="/dbvar/advanced">Advanced</a>
</li><li>
<a class="help" href="/dbvar/content/help">Help</a>
</li></ul></div>
</div>
<div class="nav_and_browser">
</div>
<!-- was itemctrl -->
<div class="container">
<div id="maincontent" class="content col twelve_col last">
<div class="col1">
<div class="dbvar-header">
<span class="info-left">
<div class="dbvar-info" id="variant_information_set"><h3>nsv4375018</h3><div class="long-info"><ul class="plain_ul"><li><span class="label">Organism: </span><a href="/Taxonomy/Browser/wwwtax.cgi?mode=Info&amp;id=9606" title="Link to Taxonomy Browser ID 9606">Homo sapiens</a></li></ul></div><span class="info"><ul class="plain_ul"><li><span class="label">Study:</span><a href="/dbvar/studies/nstd173" title="Link to Study nstd173">nstd173 (Zarrei et al. 2019)</a></li><li><span class="label">Variant Type:</span>copy number variation</li><li><span class="label">Method Type:</span>SNP array</li><li><span class="label">Submitted on:</span>GRCh37 (hg19)</li></ul></span><span class="info"><ul class="plain_ul"><li><span class="label">Variant Calls:</span>2</li><li><span class="label">Validation:</span>Not tested</li><li><span class="label">Clinical Assertions: </span>No</li><li><span class="label">Region Size:</span>141,226</li></ul></span><div class="long-info"><ul class="plain_ul"><li><span class="label">Publication(s):</span><a href="/pubmed?cmd=search&amp;term=31602316" title="Link to study Zarrei et al. 2019">Zarrei et al. 2019</a></li></ul></div></div>
</span>
<span class="info-ideo">
<div class="dbvar-ideo"><div id="ideo-container"></div><div id="ideo-comments"><span id="ideo-desc"></span><span id="ideo-legend"></span></div><link rel="stylesheet" type="text/css" href="/projects/ideogram/3.1/css/ideo.css" /><script type="text/javascript" src="/projects/ideogram/3.1/js/ideo.js"></script><script type="text/javascript">
var ideoConfig = {
index: 0,
width: 12,
height: 160,
align: "top",
labelPosition: "before",
variant: "nsv4375018",
placement:[
{
accession:"GCF_000001405.25",name:"GRCh37 (hg19)",taxid:9606,start:98025640,stop:98166865,chr:"Chr2",
dummy: null
}]
,
blockedIds: [37012]
};
</script></div>
</span>
<span class="info-right">
<!-- <component id="dbVar_Variant_FilterP"/> -->
<div class="portlet variantotherresources_portlet">
<div class="portlet_head">
<div class="portlet_title">
<h3>Links to Other Resources</h3>
</div>
<a name="PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_Variant_FilterOtherResourcesP.Shutter" sid="1" href="#" class="portlet_shutter" title="Show/hide content" remembercollapsed="true" pgsec_name="Links to Other Resources" id="PAFAppLayout.AppController.Page.dbVar_VariantPage.dbVar_Variant_FilterOtherResourcesP.Shutter"></a>
</div>
<div class="portlet_content variantotherresources_content">
<ul class="emphasis">
<li>
<a href="/gene?LinkName=dbvar_gene&amp;from_uid=49465751">
Overlapping Genes
</a>
</li>
</ul>
<div class="tertiary">Source: NCBI</div>
</div>
</div>
</span>
</div>
</div>
<!--/.col1-->
<div class="col2">
</div>
<!--/.col2-->
<div class="col3">
<div class="tabbed-contents">
<div data-jig="ncbitabs" id="dbvar-tabs"><ul><li><a id="VariantGenome1" href="#VariantGenome">Genome View</a></li><li><a id="VariantDetails1" href="#VariantDetails">Variant Region Details and Evidence</a></li><li><a id="VariantValidation1" href="#VariantValidation">Validation Information</a></li><li><a id="VariantClinical1" href="#VariantClinical">Clinical Assertions</a></li><li><a id="VariantGenotype1" href="#VariantGenotype">Genotype Information</a></li></ul><div id="VariantGenome"><script xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" type="text/javascript">
window.VariantInfo = {
variant: "nsv4375018",
title: [
"Genome View",
"Variant Region Details and Evidence",
"Validation Information",
"Clinical Assertions",
"Genotype Information"
]
};
</script><script xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" type="text/javascript" src="/projects/sviewer/js/sviewer.js" id="autoload"></script><div class="seqviewer"><div class="seqviewer-assmb"><h3>Genome View</h3><span class="seqviewer-sel"><span class="label">Select assembly:</span><select name="seqviewermenu" id="dbvar-graphics-menu"><option xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" name="accession" value="?id=NC_000002.11&amp;appname=dbvar&amp;tracks=[key:segment_map_track][key:dbvar_track,annots:NA000228605.1,linkedFeat:Packed,highlights:nsv4375018][key:gene_model_track,annots:Unnamed,Histogram:false,merge:Single%20line][key:SNP_track]&amp;noslider=1&amp;embedded=false&amp;from=98011518&amp;to=98180988" selected="selected">GRCh37 (hg19): Chr2</option></select></span><span class="seqviewer-comment"><span xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" class=""><div class="left seqviewer-comment-indent"><span class="label">Overlapping variant regions from other studies: </span><b>644</b> SVs from <b>77</b> studies. See in: <a href="/dbvar/browse/org/?taxid=9606&amp;assm=GCF_000001405.25&amp;chr=NC_000002.11&amp;from=98011518&amp;to=98180988&amp;studies=nstd173,estd1,estd188,estd192,estd194,estd195,estd197,estd199,estd20,estd201,estd203,estd209,estd210,estd212,estd214,estd217,estd219,estd229,estd231,estd24,estd55,estd59,nstd100,nstd101,nstd106,nstd107,nstd11,nstd111,nstd112,nstd113,nstd12,nstd122,nstd128,nstd130,nstd137,nstd140,nstd151,nstd152,nstd158,nstd16,nstd162,nstd168,nstd174,nstd183,nstd186,nstd195,nstd198,nstd199,nstd2,nstd200,nstd204,nstd206,nstd207,nstd209,nstd21,nstd212,nstd213,nstd214,nstd22,nstd223,nstd229,nstd237,nstd37,nstd4,nstd47,nstd49,nstd53,nstd54,nstd6,nstd65,nstd71,nstd73,nstd79,nstd82,nstd84,nstd86,nstd97,nstd99&amp;variant=nsv4375018">genome view</a>     </div><div class="right"><span class="label">Submitted genomic</span><a href="/projects/sviewer?id=NC_000002.11&amp;test=false&amp;tracks=[key:SNP_track][key:segment_map_track][key:gene_model_track,annots:Unnamed][key:dbvar_track,annots:NA000228605.1,highlights:nsv4375018]&amp;from=98011518&amp;to=98180988"><span class="range range-start">98,025,640</span>-<span class="range range-stop">98,166,865</span></a><a href="#"><img src="//static.pubmed.gov/portal/portal3rc.fcgi/4206115/img/964170" alt="Question Mark" height="14" width="14" title="Genomic location given is the largest possible for a feature. See Variant Region Details for more detailed placement information." /></a></div></span></span></div><div id="seqviewer" class="SeqViewerApp"><a href="?id=NC_000002.11&amp;appname=dbvar&amp;tracks=[key:segment_map_track][key:dbvar_track,annots:NA000228605.1,linkedFeat:Packed,highlights:nsv4375018][key:gene_model_track,annots:Unnamed,Histogram:false,merge:Single%20line][key:SNP_track]&amp;noslider=1&amp;embedded=false&amp;from=98011518&amp;to=98180988"></a></div></div></div><div id="VariantDetails"><script type="text/javascript"></script><div xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" class="info_segment" id="placement_set"><h3>Variant Region Placement Information</h3><div class="ui-ncbigrid-outer-div"><div class="ui-ncbigrid-inner-div"><table id="regplacetable" data-jig="ncbigrid" data-is-sortable="true" data-is-scrollable="false" data-column-types="[&quot;fnc:strnumSort&quot;,&quot;str&quot;, &quot;fnc:strnumSort&quot;, &quot;str&quot;, &quot;fnc:strnumSort&quot;,&quot;fnc:strnumSort&quot;,&quot;numComma&quot;,&quot;numComma&quot;,&quot;numComma&quot;,&quot;numComma&quot;,&quot;numComma&quot;,&quot;numComma&quot;]"><thead><tr><th>Variant Region ID</th><th>Placement Type</th><th>Assembly</th><th>Assembly Unit</th><th>Sequence ID</th><th>Chr</th><th>Inner Start</th><th>Inner Stop</th></tr></thead><tbody><tr><td>nsv4375018</td><td>Submitted genomic</td><td>GRCh37 (hg19)</td><td>Primary Assembly</td><td>NC_000002.11</td><td>Chr2</td><td>98,025,640</td><td>98,166,865</td></tr></tbody></table></div></div></div><div xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" class="info_segment" id="support_variant_set"><h3>Variant Call Information</h3><div class="ui-ncbigrid-outer-div"><div class="ui-ncbigrid-inner-div"><table id="calltable" class="jig-ncbigrid" data-jig="ncbigrid" data-is-scrollable="false" data-is-sortable="true" data-jigconfig="columnTypes:['str','str','str', 'str','str', 'numComma', 'str'], sortFunctions:[strnumSort,null, strnumSort, null,null, null, null]"><thead><tr><th>Variant Call ID</th><th>Type</th><th>Sample ID</th><th>Method</th><th>Analysis</th><th>Other Calls in this Sample and Study</th></tr></thead><tbody><tr><td>nssv15692650</td><td>copy number loss</td><td>OCD69-896071</td><td>SNP array</td><td>Genotyping</td><td><a href="/dbvar/?dbvartab=variant&amp;term=OCD69-896071%20AND%20nstd173" title="Retrieve full list of variant regions with calls matching this sample">22</a></td></tr><tr><td>nssv15702957</td><td>copy number loss</td><td>237508</td><td>SNP array</td><td>Genotyping</td><td><a href="/dbvar/?dbvartab=variant&amp;term=237508%20AND%20nstd173" title="Retrieve full list of variant regions with calls matching this sample">39</a></td></tr></tbody></table></div></div></div><div xmlns:ncbi-portal="http://ncbi.gov/portal/XSLT/namespace" class="info_segment" id="support_variant_placement_set"><h3>Variant Call Placement Information</h3><div class="ui-ncbigrid-outer-div"><div class="ui-ncbigrid-inner-div"><table id="callplacetable" class="jig-ncbigrid" data-jig="ncbigrid" data-is-scrollable="false" data-is-sortable="true" height="auto" data-jigconfig="columnTypes:['str','str', 'str', 'str', 'str', 'str', 'numComma', 'numComma', 'str'], sortFunctions:[strnumSort,null, null, strnumSort, strnumSort, strnumSort, null, null, null]"><thead><tr><th>Variant Call ID</th><th>Placement Type</th><th>HGVS</th><th>Assembly</th><th>Sequence ID</th><th>Chr</th><th>Inner Start</th><th>Inner Stop</th></tr></thead><tbody><tr><td>nssv15692650</td><td>Submitted genomic</td><td>NC_000002.11:g.(?_<br />98025640)_(9816686<br />5_?)del</td><td>GRCh37 (hg19)</td><td>NC_000002.11</td><td>Chr2</td><td>98,025,640</td><td>98,166,865</td></tr><tr><td>nssv15702957</td><td>Submitted genomic</td><td>NC_000002.11:g.(?_<br />98025640)_(9816686<br />5_?)del</td><td>GRCh37 (hg19)</td><td>NC_000002.11</td><td>Chr2</td><td>98,025,640</td><td>98,166,865</td></tr></tbody></table></div></div></div></div><div id="VariantValidation"><h3 class="nodata">No validation data were submitted for this variant</h3></div><div id="VariantClinical"><h3 class="nodata">No clinical assertion data were submitted for this variant</h3></div><div id="VariantGenotype"><h3 class="nodata">No genotype data were submitted for this variant</h3></div></div>
</div>
</div>
<!--/.col3-->
<div class="col4">
</div>
<!--/.col4-->
<div class="col5">
</div>
<div class="col6">
</div>
<div class="col7">
</div>
<div class="col8">
</div>
<div class="col9">
</div>
</div><!--/.content-->
</div><!--/.container-->
<div id="NCBIFooter_dynamic">
<div class="breadcrumbs">You are here:
<span id="breadcrumb_text"><a href="/guide/">NCBI</a></span></div>
<a id="help-desk-link" class="help_desk" href="https://support.ncbi.nlm.nih.gov/ics/support/default.asp?Time=2025-03-12T18:05:23-04:00&amp;Snapshot=%2Fprojects%2FdbVar%2FdbVar@9.7&amp;Host=portal107&amp;ncbi_phid=CE8E6C3C7D20094100000000005F0054&amp;ncbi_session=CE8B5AF87C7FFCB1_0191SID&amp;from=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fdbvar%2Fvariants%2Fnssv15702957%2F&amp;Ncbi_App=dbvar&amp;Page=VariantPage&amp;style=classic&amp;deptID=28049" target="_blank">Support Center</a>
<noscript><img alt="" src="/stat?jsdisabled=true&amp;ncbi_app=dbvar&amp;ncbi_db=&amp;ncbi_pdid=VariantPage&amp;ncbi_phid=CE8E6C3C7D20094100000000005F0054" /></noscript>
</div>
<div xmlns:xi="http://www.w3.org/2001/XInclude">
<xi:include href="http://127.0.0.1/sites/static/header_footer" xpointer="xmlns(x=http://www.w3.org/1999/xhtml) xpointer(//x:div[@id='footer'])"></xi:include>
</div>
<!--/.footer-->
</div>
<!--/.page-->
</div>
<!--/.wrap-->
<span class="PAFAppResources"></span>
</div><!-- /.twelve_col -->
</div>
<!-- /.grid -->
<!-- usually for JS scripts at page bottom -->
<span class="pagefixtures"></span>
<!-- CE8B5AF87C7FFCB1_0191SID /projects/dbVar/dbVar@9.7 portal107 v4.1.r689238 Tue, Oct 22 2024 16:10:51 -->
<span id="portal-csrf-token" style="display:none" data-token="CE8B5AF87C7FFCB1_0191SID"></span>
<script type='text/javascript' src='/portal/js/portal.js'></script><script type="text/javascript" src="//static.pubmed.gov/portal/portal3rc.fcgi/4206115/js/3879255/4121861/4206117/4087685/3929448/4036575/35445/31971/35962/4120814.js" snapshot="dbvar"></script></body>
</html>