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dbVar

Database of genomic structural variation

esv4141

Organism: Homo sapiens

Study:estd3 (Wang et al. 2008)
Variant Type:sequence alteration
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:463

Publication(s):Wang 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: 261 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):118,690,627-118,691,089

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
esv4141	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	118,690,627	118,691,089
esv4141	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	119,011,790	119,012,252
esv4141	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000006.10	Chr6	119,118,483	119,118,945

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
essv26582	sequence alteration	YH	Sequencing	Read depth and paired-end mapping	2,682

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
essv26582	Remapped	Perfect	GRCh38.p12	First Pass	NC_000006.12	Chr6	118,690,627	118,691,089
essv26582	Remapped	Perfect	GRCh37.p13	First Pass	NC_000006.11	Chr6	119,011,790	119,012,252
essv26582	Submitted genomic		NCBI36 (hg18)		NC_000006.10	Chr6	119,118,483	119,118,945

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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