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dbVar

Database of genomic structural variation

nsv5586014

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:77

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: 149 SVs from 41 studies. See in: genome view

Submitted genomic63,149,543-63,149,619

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5586014	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	63,149,543	63,149,619
nsv5586014	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	63,441,742	63,441,818

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17097882	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
nssv17097882	Submitted genomic		NC_000015.10:g.631 49543_63149619delG	GRCh38 (hg38)		NC_000015.10	Chr15	63,149,543	63,149,619
nssv17097882	Remapped	Perfect	NC_000015.9:g.6344 1742_63441818delG	GRCh37.p13	First Pass	NC_000015.9	Chr15	63,441,742	63,441,818

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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