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dbVar

Database of genomic structural variation

nsv5604102

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:171

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: 539 SVs from 48 studies. See in: genome view

Submitted genomic101,655,385-101,655,555

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5604102	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	101,655,385	101,655,555
nsv5604102	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	102,195,588	102,195,758

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17082912	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
nssv17082912	Submitted genomic		NC_000015.10:g.101 655385_101655555de lG	GRCh38 (hg38)		NC_000015.10	Chr15	101,655,385	101,655,555
nssv17082912	Remapped	Perfect	NC_000015.9:g.1021 95588_102195758del G	GRCh37.p13	First Pass	NC_000015.9	Chr15	102,195,588	102,195,758

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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