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dbVar

Database of genomic structural variation

nsv5935007

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:335

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: 342 SVs from 49 studies. See in: genome view

Submitted genomic9,225,120-9,225,454

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5935007	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	9,225,120	9,225,454
nsv5935007	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	9,225,118	9,225,452

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17396581	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17396581	Submitted genomic		NC_000018.10:g.922 5120_9225454del	GRCh38 (hg38)		NC_000018.10	Chr18	9,225,120	9,225,454
nssv17396581	Remapped	Perfect	NC_000018.9:g.9225 118_9225452del	GRCh37.p13	First Pass	NC_000018.9	Chr18	9,225,118	9,225,452

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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