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

dbVar

Database of genomic structural variation

nsv4639232

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:374

Description:nsv4172557 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: 111 SVs from 38 studies. See in: genome view

Remapped(Score: Perfect):98,265,323-98,265,696

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4639232	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	98,265,323	98,265,696
nsv4639232	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	100,025,080	100,025,453

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16159894	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16159894	Remapped	Perfect	NC_000010.11:g.982 65323_98265696del	GRCh38.p12	First Pass	NC_000010.11	Chr10	98,265,323	98,265,696
nssv16159894	Submitted genomic		NC_000010.10:g.100 025080_100025453de l	GRCh37 (hg19)		NC_000010.10	Chr10	100,025,080	100,025,453

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)
nssv16159894	0.256	5560	21688

You are here: NCBI