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dbVar

Database of genomic structural variation

nsv5893815

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:107

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

Submitted genomic124,289,367-124,289,473

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5893815	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	124,289,367	124,289,473
nsv5893815	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	124,008,214	124,008,320

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17395348	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17395348	Submitted genomic		NC_000003.12:g.124 289367_124289473de l	GRCh38 (hg38)		NC_000003.12	Chr3	124,289,367	124,289,473
nssv17395348	Remapped	Perfect	NC_000003.11:g.124 008214_124008320de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	124,008,214	124,008,320

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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