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

dbVar

Database of genomic structural variation

nsv5956863

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:79

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: 187 SVs from 45 studies. See in: genome view

Submitted genomic63,045,225-63,045,303

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5956863	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	63,045,225	63,045,303
nsv5956863	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	61,676,577	61,676,655

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17397964	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17397964	Submitted genomic		NC_000020.11:g.630 45225_63045303del	GRCh38 (hg38)		NC_000020.11	Chr20	63,045,225	63,045,303
nssv17397964	Remapped	Perfect	NC_000020.10:g.616 76577_61676655del	GRCh37.p13	First Pass	NC_000020.10	Chr20	61,676,577	61,676,655

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