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dbVar

Database of genomic structural variation

nsv5942933

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:799

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

Submitted genomic131,029,480-131,030,278

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5942933	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	131,029,480	131,030,278
nsv5942933	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	131,514,025	131,514,823

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17359058	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17359058	Submitted genomic		NC_000012.12:g.131 029480_131030278de l	GRCh38 (hg38)		NC_000012.12	Chr12	131,029,480	131,030,278
nssv17359058	Remapped	Perfect	NC_000012.11:g.131 514025_131514823de l	GRCh37.p13	First Pass	NC_000012.11	Chr12	131,514,025	131,514,823

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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