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

dbVar

Database of genomic structural variation

nsv5936448

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:764

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: 144 SVs from 25 studies. See in: genome view

Submitted genomic78,297,392-78,298,155

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5936448	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	78,297,392	78,298,155
nsv5936448	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	78,589,734	78,590,497

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17386424	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17386424	Submitted genomic		NC_000015.10:g.782 97392_78298155del	GRCh38 (hg38)		NC_000015.10	Chr15	78,297,392	78,298,155
nssv17386424	Remapped	Perfect	NC_000015.9:g.7858 9734_78590497del	GRCh37.p13	First Pass	NC_000015.9	Chr15	78,589,734	78,590,497

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