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

dbVar

Database of genomic structural variation

nsv6006670

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:31,803

Publication(s):Wu et al. 2021

Links to Other Resources

Overlapping Genes

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: 264 SVs from 58 studies. See in: genome view

Submitted genomic32,729,114-32,760,916

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6006670	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	32,729,114	32,760,916
nsv6006670	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	32,768,726	32,800,528

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17566939	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17566939	Submitted genomic		NC_000007.14:g.327 29114_32760916del	GRCh38 (hg38)		NC_000007.14	Chr7	32,729,114	32,760,916
nssv17566939	Remapped	Perfect	NC_000007.13:g.327 68726_32800528del	GRCh37.p13	First Pass	NC_000007.13	Chr7	32,768,726	32,800,528

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI