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dbVar

Database of genomic structural variation

nsv5891316

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:102

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: 163 SVs from 34 studies. See in: genome view

Submitted genomic141,155,967-141,156,068

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5891316	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	141,155,967	141,156,068
nsv5891316	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	142,077,121	142,077,222

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17420549	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17420549	Submitted genomic		NC_000004.12:g.141 155967_141156068de l	GRCh38 (hg38)		NC_000004.12	Chr4	141,155,967	141,156,068
nssv17420549	Remapped	Perfect	NC_000004.11:g.142 077121_142077222de l	GRCh37.p13	First Pass	NC_000004.11	Chr4	142,077,121	142,077,222

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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