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dbVar

Database of genomic structural variation

nsv5919476

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:100

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: 255 SVs from 32 studies. See in: genome view

Submitted genomic130,245,574-130,245,673

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5919476	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	130,245,574	130,245,673
nsv5919476	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	130,115,469	130,115,568

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17367987	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17367987	Submitted genomic		NC_000011.10:g.130 245574_130245673de l	GRCh38 (hg38)		NC_000011.10	Chr11	130,245,574	130,245,673
nssv17367987	Remapped	Perfect	NC_000011.9:g.1301 15469_130115568del	GRCh37.p13	First Pass	NC_000011.9	Chr11	130,115,469	130,115,568

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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