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dbVar

Database of genomic structural variation

nsv5593228

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:80

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: 646 SVs from 61 studies. See in: genome view

Submitted genomic30,929,717-30,929,796

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5593228	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	30,929,717	30,929,796
nsv5593228	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	31,221,920	31,221,999

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17088335	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
nssv17088335	Submitted genomic		NC_000015.10:g.309 29717_30929796delT	GRCh38 (hg38)		NC_000015.10	Chr15	30,929,717	30,929,796
nssv17088335	Remapped	Perfect	NC_000015.9:g.3122 1920_31221999delT	GRCh37.p13	First Pass	NC_000015.9	Chr15	31,221,920	31,221,999

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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