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dbVar

Database of genomic structural variation

nsv5919424

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:5,280

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: 154 SVs from 45 studies. See in: genome view

Submitted genomic34,199,214-34,204,493

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5919424	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	34,199,214	34,204,493
nsv5919424	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	34,220,761	34,226,040

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17361966	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17361966	Submitted genomic		NC_000011.10:g.341 99214_34204493del	GRCh38 (hg38)		NC_000011.10	Chr11	34,199,214	34,204,493
nssv17361966	Remapped	Perfect	NC_000011.9:g.3422 0761_34226040del	GRCh37.p13	First Pass	NC_000011.9	Chr11	34,220,761	34,226,040

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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