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

dbVar

Database of genomic structural variation

nsv5915984

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:624

Publication(s):Almarri et al. 2020

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: 133 SVs from 29 studies. See in: genome view

Submitted genomic131,540,887-131,541,510

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5915984	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	131,540,887	131,541,510
nsv5915984	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	131,225,646	131,226,269

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17443690	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17443690	Submitted genomic		NC_000007.14:g.131 540887_131541510de l	GRCh38 (hg38)		NC_000007.14	Chr7	131,540,887	131,541,510
nssv17443690	Remapped	Perfect	NC_000007.13:g.131 225646_131226269de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	131,225,646	131,226,269

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