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dbVar

Database of genomic structural variation

esv2095170

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: 114 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):79,400,086-79,400,086

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv2095170	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	79,400,086	79,400,086
esv2095170	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	78,695,909	78,695,909
esv2095170	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000005.8	Chr5	78,731,665	78,731,665

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv4738974	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
essv4738974	Remapped	Perfect	NC_000005.10:g.794 00086_79400087insT	GRCh38.p12	First Pass	NC_000005.10	Chr5	79,400,086	79,400,086
essv4738974	Remapped	Perfect	NC_000005.9:g.7869 5909_78695910insT	GRCh37.p13	First Pass	NC_000005.9	Chr5	78,695,909	78,695,909
essv4738974	Submitted genomic		NC_000005.8:g.7873 1665_78731666insT	NCBI36 (hg18)		NC_000005.8	Chr5	78,731,665	78,731,665

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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