A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615793



Internal ID21564098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31706921..31706921hg38UCSC Ensembl
chr3:31748413..31748413hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381536
hg191536
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137601
SamplesHG01596
Known GenesOSBPL10, OSBPL10-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615793
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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