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dbVar

Database of genomic structural variation

nsv5928387

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:132

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: 105 SVs from 24 studies. See in: genome view

Submitted genomic40,356,113-40,356,244

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5928387	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	40,356,113	40,356,244
nsv5928387	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	40,648,314	40,648,445

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17373768	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17373768	Submitted genomic		NC_000015.10:g.403 56113_40356244del	GRCh38 (hg38)		NC_000015.10	Chr15	40,356,113	40,356,244
nssv17373768	Remapped	Perfect	NC_000015.9:g.4064 8314_40648445del	GRCh37.p13	First Pass	NC_000015.9	Chr15	40,648,314	40,648,445

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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