A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5993066



Internal ID21902409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23871763..23872974hg38UCSC Ensembl
chr3:23913254..23914465hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381212
hg191212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547779
Samples
Known GenesUBE2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5993066
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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