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dbVar

Database of genomic structural variation

nsv6025812

Organism: Homo sapiens

Study:nstd212 (Wu 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:78

Publication(s):Wu 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: 112 SVs from 23 studies. See in: genome view

Submitted genomic40,897,177-40,897,254

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6025812	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	40,897,177	40,897,254
nsv6025812	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	41,189,375	41,189,452

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17600565	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17600565	Submitted genomic		NC_000015.10:g.408 97177_40897254del	GRCh38 (hg38)		NC_000015.10	Chr15	40,897,177	40,897,254
nssv17600565	Remapped	Perfect	NC_000015.9:g.4118 9375_41189452del	GRCh37.p13	First Pass	NC_000015.9	Chr15	41,189,375	41,189,452

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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