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dbVar

Database of genomic structural variation

nsv6121777

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:299

Description:nsv5498236 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: 244 SVs from 39 studies. See in: genome view

Remapped(Score: Perfect):110,160,161-110,160,459

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6121777	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	110,160,161	110,160,459
nsv6121777	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	110,812,508	110,812,806

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17963254	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17963254	Remapped	Perfect	NC_000013.11:g.110 160161_110160459de l	GRCh38.p12	First Pass	NC_000013.11	Chr13	110,160,161	110,160,459
nssv17963254	Submitted genomic		NC_000013.10:g.110 812508_110812806de l	GRCh37 (hg19)		NC_000013.10	Chr13	110,812,508	110,812,806

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)
nssv17963254	0.16	1024	6404

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