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dbVar

Database of genomic structural variation

nsv5895357

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:93

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: 155 SVs from 31 studies. See in: genome view

Submitted genomic141,219,431-141,219,523

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5895357	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	141,219,431	141,219,523
nsv5895357	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	142,140,585	142,140,677

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17417512	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17417512	Submitted genomic		NC_000004.12:g.141 219431_141219523de l	GRCh38 (hg38)		NC_000004.12	Chr4	141,219,431	141,219,523
nssv17417512	Remapped	Perfect	NC_000004.11:g.142 140585_142140677de l	GRCh37.p13	First Pass	NC_000004.11	Chr4	142,140,585	142,140,677

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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