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dbVar

Database of genomic structural variation

nsv5599374

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:64

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: 140 SVs from 27 studies. See in: genome view

Submitted genomic36,703,341-36,703,404

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5599374	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	36,703,341	36,703,404
nsv5599374	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	36,995,542	36,995,605

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17085881	deletion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17085881	Submitted genomic		NC_000015.10:g.367 03341_36703404delC	GRCh38 (hg38)		NC_000015.10	Chr15	36,703,341	36,703,404
nssv17085881	Remapped	Perfect	NC_000015.9:g.3699 5542_36995605delC	GRCh37.p13	First Pass	NC_000015.9	Chr15	36,995,542	36,995,605

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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