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dbVar

Database of genomic structural variation

nsv5936969

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:1,986

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: 216 SVs from 25 studies. See in: genome view

Submitted genomic35,687,182-35,689,167

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5936969	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	35,687,182	35,689,167
nsv5936969	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	33,267,146	33,269,131

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17384439	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17384439	Submitted genomic		NC_000018.10:g.356 87182_35689167del	GRCh38 (hg38)		NC_000018.10	Chr18	35,687,182	35,689,167
nssv17384439	Remapped	Perfect	NC_000018.9:g.3326 7146_33269131del	GRCh37.p13	First Pass	NC_000018.9	Chr18	33,267,146	33,269,131

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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