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dbVar

Database of genomic structural variation

nsv5909992

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:7,568,594

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: 17274 SVs from 130 studies. See in: genome view

Submitted genomic72,964,663-80,533,256

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5909992	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	72,964,663	80,533,256
nsv5909992	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	74,724,421	82,293,012

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17366271	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17366271	Submitted genomic		NC_000010.11:g.729 64663_80533256del	GRCh38 (hg38)		NC_000010.11	Chr10	72,964,663	80,533,256
nssv17366271	Remapped	Perfect	NC_000010.10:g.747 24421_82293012del	GRCh37.p13	First Pass	NC_000010.10	Chr10	74,724,421	82,293,012

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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