Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6113183

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:98,001

Description:nsv5423441 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: 418 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):56,673,388-56,771,388

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6113183	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000024.10	ChrY	56,673,388	56,771,388
nsv6113183	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000024.9	ChrY	58,819,483	58,917,483

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17968517	copy number variation	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17968517	Remapped	Perfect	GRCh38.p12	First Pass	NC_000024.10	ChrY	56,673,388	56,771,388
nssv17968517	Submitted genomic		GRCh37 (hg19)		NC_000024.9	ChrY	58,819,483	58,917,483

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)
nssv17968517	0.5	1598	3196

You are here: NCBI