A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114439



Internal ID21297705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:23807475..23812181hg38UCSC Ensembl
Innerchr3:23848966..23853672hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg384707
hg194707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14108540
Samplessample357
Known GenesUBE2E1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114439
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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