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dbVar

Database of genomic structural variation

nsv5914966

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:316

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: 193 SVs from 60 studies. See in: genome view

Submitted genomic31,130,884-31,131,199

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5914966	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	31,130,884	31,131,199
nsv5914966	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	31,152,431	31,152,746

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17350712	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17350712	Submitted genomic		NC_000011.10:g.311 30884_31131199del	GRCh38 (hg38)		NC_000011.10	Chr11	31,130,884	31,131,199
nssv17350712	Remapped	Perfect	NC_000011.9:g.3115 2431_31152746del	GRCh37.p13	First Pass	NC_000011.9	Chr11	31,152,431	31,152,746

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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