A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110299



Internal ID21293565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33589340..33596189hg38UCSC Ensembl
Innerchr20:32177146..32183995hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg386850
hg196850
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv685n145
Supporting Variantsnssv14100733
Samplessample350
Known GenesCBFA2T2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110299
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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