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dbVar

Database of genomic structural variation

nsv5935197

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:378

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: 164 SVs from 17 studies. See in: genome view

Submitted genomic21,091,539-21,091,916

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5935197	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	21,091,539	21,091,916
nsv5935197	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	18,671,500	18,671,877

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17370585	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17370585	Submitted genomic		NC_000018.10:g.210 91539_21091916del	GRCh38 (hg38)		NC_000018.10	Chr18	21,091,539	21,091,916
nssv17370585	Remapped	Perfect	NC_000018.9:g.1867 1500_18671877del	GRCh37.p13	First Pass	NC_000018.9	Chr18	18,671,500	18,671,877

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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