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dbVar

Database of genomic structural variation

nsv5944875

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:720

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: 237 SVs from 37 studies. See in: genome view

Submitted genomic97,459,431-97,460,150

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5944875	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	97,459,431	97,460,150
nsv5944875	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	98,002,661	98,003,380

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17382761	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17382761	Submitted genomic		NC_000015.10:g.974 59431_97460150del	GRCh38 (hg38)		NC_000015.10	Chr15	97,459,431	97,460,150
nssv17382761	Remapped	Perfect	NC_000015.9:g.9800 2661_98003380del	GRCh37.p13	First Pass	NC_000015.9	Chr15	98,002,661	98,003,380

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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