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dbVar

Database of genomic structural variation

nsv5592502

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:269

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: 113 SVs from 31 studies. See in: genome view

Submitted genomic95,809,828-95,810,096

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5592502	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	95,809,828	95,810,096
nsv5592502	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	97,569,585	97,569,853

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17072053	deletion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17072053	Submitted genomic		NC_000010.11:g.958 09828_95810096delG	GRCh38 (hg38)		NC_000010.11	Chr10	95,809,828	95,810,096
nssv17072053	Remapped	Perfect	NC_000010.10:g.975 69585_97569853delG	GRCh37.p13	First Pass	NC_000010.10	Chr10	97,569,585	97,569,853

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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