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dbVar

Database of genomic structural variation

nsv5573646

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:130

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: 220 SVs from 55 studies. See in: genome view

Submitted genomic55,763,718-55,763,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5573646	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	55,763,718	55,763,847
nsv5573646	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	56,676,277	56,676,406

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17149135	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17149135	Submitted genomic		NC_000008.11:g.557 63718_55763847delA	GRCh38 (hg38)		NC_000008.11	Chr8	55,763,718	55,763,847
nssv17149135	Remapped	Perfect	NC_000008.10:g.566 76277_56676406delA	GRCh37.p13	First Pass	NC_000008.10	Chr8	56,676,277	56,676,406

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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