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dbVar

Database of genomic structural variation

nsv6122320

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:184

Description:nsv5504305 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: 327 SVs from 52 studies. See in: genome view

Remapped(Score: Perfect):113,812,759-113,812,942

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6122320	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	113,812,759	113,812,942
nsv6122320	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	114,515,732	114,515,915

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17963330	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17963330	Remapped	Perfect	NC_000013.11:g.113 812759_113812942du p	GRCh38.p12	First Pass	NC_000013.11	Chr13	113,812,759	113,812,942
nssv17963330	Submitted genomic		NC_000013.10:g.114 515732_114515915du p	GRCh37 (hg19)		NC_000013.10	Chr13	114,515,732	114,515,915

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)
nssv17963330	0.117	750	6404

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