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dbVar

Database of genomic structural variation

nsv5933382

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:74

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: 103 SVs from 20 studies. See in: genome view

Submitted genomic58,252,948-58,253,021

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5933382	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	58,252,948	58,253,021
nsv5933382	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	58,719,666	58,719,739

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17369805	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17369805	Submitted genomic		NC_000014.9:g.5825 2948_58253021del	GRCh38 (hg38)		NC_000014.9	Chr14	58,252,948	58,253,021
nssv17369805	Remapped	Perfect	NC_000014.8:g.5871 9666_58719739del	GRCh37.p13	First Pass	NC_000014.8	Chr14	58,719,666	58,719,739

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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