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

dbVar

Database of genomic structural variation

nsv6016125

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:190,465

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: 472 SVs from 56 studies. See in: genome view

Submitted genomic120,078,331-120,268,795

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6016125	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	120,078,331	120,268,795
nsv6016125	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	119,718,385	119,908,849

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17574361	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17574361	Submitted genomic		NC_000007.14:g.120 078331_120268795du p	GRCh38 (hg38)		NC_000007.14	Chr7	120,078,331	120,268,795
nssv17574361	Remapped	Perfect	NC_000007.13:g.119 718385_119908849du p	GRCh37.p13	First Pass	NC_000007.13	Chr7	119,718,385	119,908,849

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