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dbVar

Database of genomic structural variation

nsv5900963

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:649,704

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: 2586 SVs from 100 studies. See in: genome view

Submitted genomic63,585,802-64,235,505

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5900963	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	63,585,802	64,235,505
nsv5900963	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	64,451,520	65,101,223

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17426001	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17426001	Submitted genomic		NC_000004.12:g.635 85802_64235505del	GRCh38 (hg38)		NC_000004.12	Chr4	63,585,802	64,235,505
nssv17426001	Remapped	Perfect	NC_000004.11:g.644 51520_65101223del	GRCh37.p13	First Pass	NC_000004.11	Chr4	64,451,520	65,101,223

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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