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

dbVar

Database of genomic structural variation

nsv4656385

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:58,061

Description:esv3826083 from 1000 Genomes Consortium Phase 3 Integrated SV. 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: 322 SVs from 57 studies. See in: genome view

Remapped(Score: Perfect):130,574,984-130,633,044

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4656385	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	130,574,984	130,633,044
nsv4656385	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	131,332,557	131,390,617

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16181495	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16181495	Remapped	Perfect	NC_000002.12:g.130 574984_130633044de l	GRCh38.p12	First Pass	NC_000002.12	Chr2	130,574,984	130,633,044
nssv16181495	Submitted genomic		NC_000002.11:g.131 332557_131390617de l	GRCh37 (hg19)		NC_000002.11	Chr2	131,332,557	131,390,617

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)
nssv16181495	0.035	176	5008

You are here: NCBI