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dbVar

Database of genomic structural variation

esv2281059

Organism: Homo sapiens

Study:estd194 (Bentley et al. 2008)
Variant Type:insertion
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Bentley et al. 2008

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 120 SVs from 26 studies. See in: genome view

Remapped(Score: Perfect):93,151,463-93,151,463

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv2281059	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	93,151,463	93,151,463
esv2281059	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	93,694,692	93,694,692
esv2281059	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000015.8	Chr15	91,495,696	91,495,696

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv5001891	insertion	NA18507	Sequencing	Split read mapping	504,912

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv5001891	Remapped	Perfect	NC_000015.10:g.931 51463_93151464insT	GRCh38.p12	First Pass	NC_000015.10	Chr15	93,151,463	93,151,463
essv5001891	Remapped	Perfect	NC_000015.9:g.9369 4692_93694693insT	GRCh37.p13	First Pass	NC_000015.9	Chr15	93,694,692	93,694,692
essv5001891	Submitted genomic		NC_000015.8:g.9149 5696_91495697insT	NCBI36 (hg18)		NC_000015.8	Chr15	91,495,696	91,495,696

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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