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dbVar

Database of genomic structural variation

nsv5595306

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:1,151

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: 142 SVs from 28 studies. See in: genome view

Submitted genomic62,792,591-62,793,741

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5595306	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	62,792,591	62,793,741
nsv5595306	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	60,869,952	60,871,102

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17080346	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
nssv17080346	Submitted genomic		NC_000017.11:g.627 92591_62793741delC	GRCh38 (hg38)		NC_000017.11	Chr17	62,792,591	62,793,741
nssv17080346	Remapped	Perfect	NC_000017.10:g.608 69952_60871102delC	GRCh37.p13	First Pass	NC_000017.10	Chr17	60,869,952	60,871,102

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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