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

dbVar

Database of genomic structural variation

nsv5957943

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:2,485

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: 112 SVs from 21 studies. See in: genome view

Submitted genomic20,707,799-20,710,283

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5957943	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	20,707,799	20,710,283
nsv5957943	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	20,688,442	20,690,926

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17404866	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17404866	Submitted genomic		NC_000020.11:g.207 07799_20710283del	GRCh38 (hg38)		NC_000020.11	Chr20	20,707,799	20,710,283
nssv17404866	Remapped	Perfect	NC_000020.10:g.206 88442_20690926del	GRCh37.p13	First Pass	NC_000020.10	Chr20	20,688,442	20,690,926

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