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dbVar

Database of genomic structural variation

nsv4650436

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:51,079

Description:nsv4178358 from gnomAD Structural Variants. 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: 1088 SVs from 70 studies. See in: genome view

Remapped(Score: Pass):42,340,041-42,391,119

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4650436	Remapped	Pass	GRCh38.p12	Primary Assembly	First Pass	NC_000009.12	Chr9	42,340,041	42,391,119
nsv4650436	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000009.11	Chr9	44,580,000	44,640,500

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16156180	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16156180	Remapped	Pass	NC_000009.12:g.423 40041_42391119del	GRCh38.p12	First Pass	NC_000009.12	Chr9	42,340,041	42,391,119
nssv16156180	Submitted genomic		NC_000009.11:g.445 80000_44640500del	GRCh37 (hg19)		NC_000009.11	Chr9	44,580,000	44,640,500

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)
nssv16156180	0.511	11082	21694

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