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dbVar

Database of genomic structural variation

nsv5923527

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:2,567

Publication(s):Almarri et al. 2020

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: 123 SVs from 24 studies. See in: genome view

Submitted genomic109,260,393-109,262,959

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5923527	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	109,260,393	109,262,959
nsv5923527	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	112,022,673	112,025,239

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17438799	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17438799	Submitted genomic		NC_000009.12:g.109 260393_109262959de l	GRCh38 (hg38)		NC_000009.12	Chr9	109,260,393	109,262,959
nssv17438799	Remapped	Perfect	NC_000009.11:g.112 022673_112025239de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	112,022,673	112,025,239

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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