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dbVar

Database of genomic structural variation

nsv5597906

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:65

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: 133 SVs from 26 studies. See in: genome view

Submitted genomic7,593,768-7,593,832

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5597906	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	7,593,768	7,593,832
nsv5597906	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	7,635,731	7,635,795

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17071308	deletion	HG03065	Sequencing	Sequence alignment	3,836

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17071308	Submitted genomic		NC_000010.11:g.759 3768_7593832delA	GRCh38 (hg38)		NC_000010.11	Chr10	7,593,768	7,593,832
nssv17071308	Remapped	Perfect	NC_000010.10:g.763 5731_7635795delA	GRCh37.p13	First Pass	NC_000010.10	Chr10	7,635,731	7,635,795

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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