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dbVar

Database of genomic structural variation

nsv5895422

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:286

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

Submitted genomic159,519,523-159,519,808

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5895422	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	159,519,523	159,519,808
nsv5895422	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	160,376,034	160,376,319

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17404698	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17404698	Submitted genomic		NC_000002.12:g.159 519523_159519808de l	GRCh38 (hg38)		NC_000002.12	Chr2	159,519,523	159,519,808
nssv17404698	Remapped	Perfect	NC_000002.11:g.160 376034_160376319de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	160,376,034	160,376,319

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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