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dbVar

Database of genomic structural variation

nsv5919380

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:50

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

Submitted genomic13,921,341-13,921,390

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5919380	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	13,921,341	13,921,390
nsv5919380	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	13,942,888	13,942,937

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17356692	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17356692	Submitted genomic		NC_000011.10:g.139 21341_13921390del	GRCh38 (hg38)		NC_000011.10	Chr11	13,921,341	13,921,390
nssv17356692	Remapped	Perfect	NC_000011.9:g.1394 2888_13942937del	GRCh37.p13	First Pass	NC_000011.9	Chr11	13,942,888	13,942,937

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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