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dbVar

Database of genomic structural variation

nsv5934517

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:310

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: 110 SVs from 21 studies. See in: genome view

Submitted genomic40,707,243-40,707,552

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5934517	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	40,707,243	40,707,552
nsv5934517	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	40,999,441	40,999,750

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17381932	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17381932	Submitted genomic		NC_000015.10:g.407 07243_40707552del	GRCh38 (hg38)		NC_000015.10	Chr15	40,707,243	40,707,552
nssv17381932	Remapped	Perfect	NC_000015.9:g.4099 9441_40999750del	GRCh37.p13	First Pass	NC_000015.9	Chr15	40,999,441	40,999,750

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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