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dbVar

Database of genomic structural variation

nsv5921764

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:124

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

Submitted genomic80,134,710-80,134,833

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5921764	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	80,134,710	80,134,833
nsv5921764	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	81,894,466	81,894,589

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17363694	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17363694	Submitted genomic		NC_000010.11:g.801 34710_80134833del	GRCh38 (hg38)		NC_000010.11	Chr10	80,134,710	80,134,833
nssv17363694	Remapped	Perfect	NC_000010.10:g.818 94466_81894589del	GRCh37.p13	First Pass	NC_000010.10	Chr10	81,894,466	81,894,589

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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