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dbVar

Database of genomic structural variation

nsv5945264

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:78

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: 164 SVs from 30 studies. See in: genome view

Submitted genomic33,643,558-33,643,635

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5945264	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	33,643,558	33,643,635
nsv5945264	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	33,935,759	33,935,836

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17384824	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17384824	Submitted genomic		NC_000015.10:g.336 43558_33643635del	GRCh38 (hg38)		NC_000015.10	Chr15	33,643,558	33,643,635
nssv17384824	Remapped	Perfect	NC_000015.9:g.3393 5759_33935836del	GRCh37.p13	First Pass	NC_000015.9	Chr15	33,935,759	33,935,836

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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