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dbVar

Database of genomic structural variation

nsv5596311

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:316

Publication(s):Ebert et al. 2021

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: 152 SVs from 34 studies. See in: genome view

Submitted genomic43,739,797-43,740,112

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5596311	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	43,739,797	43,740,112
nsv5596311	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	44,031,995	44,032,310

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17092533	deletion	HG02818	Sequencing	Sequence alignment	3,473

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17092533	Submitted genomic		NC_000015.10:g.437 39797_43740112delT	GRCh38 (hg38)		NC_000015.10	Chr15	43,739,797	43,740,112
nssv17092533	Remapped	Perfect	NC_000015.9:g.4403 1995_44032310delT	GRCh37.p13	First Pass	NC_000015.9	Chr15	44,031,995	44,032,310

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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