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dbVar

Database of genomic structural variation

nsv5586066

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:321

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: 165 SVs from 33 studies. See in: genome view

Submitted genomic33,747,322-33,747,642

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5586066	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	33,747,322	33,747,642
nsv5586066	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	32,335,128	32,335,448

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17116534	deletion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17116534	Submitted genomic		NC_000020.11:g.337 47322_33747642delA	GRCh38 (hg38)		NC_000020.11	Chr20	33,747,322	33,747,642
nssv17116534	Remapped	Perfect	NC_000020.10:g.323 35128_32335448delA	GRCh37.p13	First Pass	NC_000020.10	Chr20	32,335,128	32,335,448

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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