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dbVar

Database of genomic structural variation

nsv5594332

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

Submitted genomic29,558,512-29,558,569

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5594332	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	29,558,512	29,558,569
nsv5594332	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	30,132,649	30,132,706

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17081219	deletion	SAMN00006466	Sequencing	Sequence alignment	4,625

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17081219	Submitted genomic		NC_000013.11:g.295 58512_29558569delA	GRCh38 (hg38)		NC_000013.11	Chr13	29,558,512	29,558,569
nssv17081219	Remapped	Perfect	NC_000013.10:g.301 32649_30132706delA	GRCh37.p13	First Pass	NC_000013.10	Chr13	30,132,649	30,132,706

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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