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dbVar

Database of genomic structural variation

nsv5886332

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:71

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: 138 SVs from 27 studies. See in: genome view

Submitted genomic15,098,117-15,098,187

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5886332	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	15,098,117	15,098,187
nsv5886332	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	15,238,241	15,238,311

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17402681	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17402681	Submitted genomic		NC_000002.12:g.150 98117_15098187del	GRCh38 (hg38)		NC_000002.12	Chr2	15,098,117	15,098,187
nssv17402681	Remapped	Perfect	NC_000002.11:g.152 38241_15238311del	GRCh37.p13	First Pass	NC_000002.11	Chr2	15,238,241	15,238,311

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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