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dbVar

Database of genomic structural variation

nsv5880365

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:197

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: 176 SVs from 28 studies. See in: genome view

Submitted genomic46,107,314-46,107,510

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5880365	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	46,107,314	46,107,510
nsv5880365	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	46,572,986	46,573,182

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17386547	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17386547	Submitted genomic		NC_000001.11:g.461 07314_46107510del	GRCh38 (hg38)		NC_000001.11	Chr1	46,107,314	46,107,510
nssv17386547	Remapped	Perfect	NC_000001.10:g.465 72986_46573182del	GRCh37.p13	First Pass	NC_000001.10	Chr1	46,572,986	46,573,182

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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