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dbVar

Database of genomic structural variation

nsv5945076

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:67

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: 303 SVs from 34 studies. See in: genome view

Submitted genomic107,708,511-107,708,577

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5945076	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	107,708,511	107,708,577
nsv5945076	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	108,360,859	108,360,925

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17364767	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17364767	Submitted genomic		NC_000013.11:g.107 708511_107708577de l	GRCh38 (hg38)		NC_000013.11	Chr13	107,708,511	107,708,577
nssv17364767	Remapped	Perfect	NC_000013.10:g.108 360859_108360925de l	GRCh37.p13	First Pass	NC_000013.10	Chr13	108,360,859	108,360,925

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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