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dbVar

Database of genomic structural variation

nsv5570002

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:2,441

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: 126 SVs from 32 studies. See in: genome view

Submitted genomic107,795,459-107,797,899

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5570002	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	107,795,459	107,797,899
nsv5570002	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	107,435,904	107,438,344

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17154174	deletion	HG02011	Sequencing	Sequence alignment	2,906

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17154174	Submitted genomic		NC_000007.14:g.107 795459_107797899de lA	GRCh38 (hg38)		NC_000007.14	Chr7	107,795,459	107,797,899
nssv17154174	Remapped	Perfect	NC_000007.13:g.107 435904_107438344de lA	GRCh37.p13	First Pass	NC_000007.13	Chr7	107,435,904	107,438,344

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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