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dbVar

Database of genomic structural variation

nsv6116473

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:236,521

Description:nsv5417888 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: 1896 SVs from 86 studies. See in: genome view

Remapped(Score: Perfect):46,291,980-46,528,500

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6116473	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	46,291,980	46,528,500
nsv6116473	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	44,369,346	44,605,866

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17958028	copy number variation	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17958028	Remapped	Perfect	GRCh38.p12	First Pass	NC_000017.11	Chr17	46,291,980	46,528,500
nssv17958028	Submitted genomic		GRCh37 (hg19)		NC_000017.10	Chr17	44,369,346	44,605,866

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)
nssv17958028	0.424	1185	2792

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