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

dbVar

Database of genomic structural variation

nsv5941649

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:438

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: 115 SVs from 24 studies. See in: genome view

Submitted genomic32,086,493-32,086,930

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5941649	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	32,086,493	32,086,930
nsv5941649	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	32,555,699	32,556,136

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17376681	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17376681	Submitted genomic		NC_000014.9:g.3208 6493_32086930del	GRCh38 (hg38)		NC_000014.9	Chr14	32,086,493	32,086,930
nssv17376681	Remapped	Perfect	NC_000014.8:g.3255 5699_32556136del	GRCh37.p13	First Pass	NC_000014.8	Chr14	32,555,699	32,556,136

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