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dbVar

Database of genomic structural variation

nsv5567635

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:58

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: 467 SVs from 52 studies. See in: genome view

Submitted genomic186,547,065-186,547,122

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5567635	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	186,547,065	186,547,122
nsv5567635	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	187,468,219	187,468,276

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17121526	deletion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17121526	Submitted genomic		NC_000004.12:g.186 547065_186547122de lC	GRCh38 (hg38)		NC_000004.12	Chr4	186,547,065	186,547,122
nssv17121526	Remapped	Perfect	NC_000004.11:g.187 468219_187468276de lC	GRCh37.p13	First Pass	NC_000004.11	Chr4	187,468,219	187,468,276

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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