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dbVar

Database of genomic structural variation

nsv5952950

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:699,360

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: 2330 SVs from 82 studies. See in: genome view

Submitted genomic34,143,842-34,843,201

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5952950	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	34,143,842	34,843,201
nsv5952950	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	32,731,648	33,431,004

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17402925	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17402925	Submitted genomic		NC_000020.11:g.341 43842_34843201del	GRCh38 (hg38)		NC_000020.11	Chr20	34,143,842	34,843,201
nssv17402925	Remapped	Perfect	NC_000020.10:g.327 31648_33431004del	GRCh37.p13	First Pass	NC_000020.10	Chr20	32,731,648	33,431,004

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.

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