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dbVar

Database of genomic structural variation

nsv5670832

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:14,995

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

Submitted genomic108,364,720-108,379,714

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5670832	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	108,364,720	108,379,714
nsv5670832	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	107,607,950	107,622,944

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17164891	deletion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17164891	Submitted genomic		NC_000023.11:g.108 364720_108379714de lG	GRCh38 (hg38)		NC_000023.11	ChrX	108,364,720	108,379,714
nssv17164891	Remapped	Perfect	NC_000023.10:g.107 607950_107622944de lG	GRCh37.p13	First Pass	NC_000023.10	ChrX	107,607,950	107,622,944

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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