A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549592



Internal ID21873947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23871559..23871833hg38UCSC Ensembl
chr3:23913050..23913324hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993298
Supporting Variants
Samples
Known GenesUBE2E1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549592
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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