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dbVar

Database of genomic structural variation

nsv5598917

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:114

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: 254 SVs from 36 studies. See in: genome view

Submitted genomic79,372,873-79,372,986

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5598917	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	79,372,873	79,372,986
nsv5598917	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	79,947,008	79,947,121

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17092178	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
nssv17092178	Submitted genomic		NC_000013.11:g.793 72873_79372986delA	GRCh38 (hg38)		NC_000013.11	Chr13	79,372,873	79,372,986
nssv17092178	Remapped	Perfect	NC_000013.10:g.799 47008_79947121delA	GRCh37.p13	First Pass	NC_000013.10	Chr13	79,947,008	79,947,121

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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