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dbVar

Database of genomic structural variation

nsv5923390

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:1,150

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: 125 SVs from 29 studies. See in: genome view

Submitted genomic88,502,476-88,503,625

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5923390	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	88,502,476	88,503,625
nsv5923390	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	88,235,644	88,236,793

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17366613	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17366613	Submitted genomic		NC_000011.10:g.885 02476_88503625del	GRCh38 (hg38)		NC_000011.10	Chr11	88,502,476	88,503,625
nssv17366613	Remapped	Perfect	NC_000011.9:g.8823 5644_88236793del	GRCh37.p13	First Pass	NC_000011.9	Chr11	88,235,644	88,236,793

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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