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dbVar

Database of genomic structural variation

nsv6307593

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:44,001

Description:nsv6145803 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: 539 SVs from 74 studies. See in: genome view

Remapped(Score: Perfect):32,307,874-32,351,874

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6307593	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	32,307,874	32,351,874
nsv6307593	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	32,600,075	32,644,075

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17967549	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17967549	Remapped	Perfect	NC_000015.10:g.323 07874_32351874del	GRCh38.p12	First Pass	NC_000015.10	Chr15	32,307,874	32,351,874
nssv17967549	Submitted genomic		NC_000015.9:g.3260 0075_32644075del	GRCh37 (hg19)		NC_000015.9	Chr15	32,600,075	32,644,075

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)
nssv17967549	0.017	93	5608

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