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dbVar

Database of genomic structural variation

nsv5942307

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:409

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: 159 SVs from 20 studies. See in: genome view

Submitted genomic90,546,922-90,547,330

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5942307	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	90,546,922	90,547,330
nsv5942307	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	91,090,154	91,090,562

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17383922	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17383922	Submitted genomic		NC_000015.10:g.905 46922_90547330del	GRCh38 (hg38)		NC_000015.10	Chr15	90,546,922	90,547,330
nssv17383922	Remapped	Perfect	NC_000015.9:g.9109 0154_91090562del	GRCh37.p13	First Pass	NC_000015.9	Chr15	91,090,154	91,090,562

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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