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dbVar

Database of genomic structural variation

nsv5916005

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:153

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: 322 SVs from 46 studies. See in: genome view

Submitted genomic132,047,666-132,047,818

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5916005	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	132,047,666	132,047,818
nsv5916005	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	133,861,170	133,861,322

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17362949	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17362949	Submitted genomic		NC_000010.11:g.132 047666_132047818de l	GRCh38 (hg38)		NC_000010.11	Chr10	132,047,666	132,047,818
nssv17362949	Remapped	Perfect	NC_000010.10:g.133 861170_133861322de l	GRCh37.p13	First Pass	NC_000010.10	Chr10	133,861,170	133,861,322

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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