nih-gov/www.ncbi.nlm.nih.gov/data_specs/schema/other/dbvar

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<title>Index of dbvar</title>
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<h1>Index of <i>dbvar</i> :</h1>
<img src="/icons/back.gif" alt="[DIR]" /><a href="..">Parent directory</a>
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<p>&nbsp;&nbsp;
This is a XML Schema specification for submission to
<a href="https://www.ncbi.nlm.nih.gov/projects/dbvar">dbVar</a>.
<br />&nbsp;&nbsp;
dbVar is a database for genomic structural variation and we accept submissions of data involving
any regions of DNA in inversions and balanced translocations or genomic imbalances
(insertions and deletions), commonly referred to as copy number variants (CNVs).
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<tr><th></th><th>Name</th><th>Last modified</th><th>Size</th></tr>
<tr><td><img src="/icons/generic.gif" alt="[ ]" /></td><td><a href="dbVar.xsd">dbVar.xsd</a></td><td>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;2020-04-21 23:03</td><td align="right">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;107528</td></tr>
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