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dbVar

Database of genomic structural variation

nsv6297382

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:155,491

Description:nsv5473731 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 563 SVs from 70 studies. See in: genome view

Remapped(Score: Perfect):97,653,930-97,809,420

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6297382	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	97,653,930	97,809,420
nsv6297382	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	98,575,081	98,730,571

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17664633	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17664633	Remapped	Perfect	NC_000004.12:g.976 53930_97809420del	GRCh38.p12	First Pass	NC_000004.12	Chr4	97,653,930	97,809,420
nssv17664633	Submitted genomic		NC_000004.11:g.985 75081_98730571del	GRCh37 (hg19)		NC_000004.11	Chr4	98,575,081	98,730,571

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17664633	0.751	4809	6404

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