A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111812



Internal ID21295078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33588592..33596189hg38UCSC Ensembl
Innerchr20:32176398..32183995hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387598
hg197598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv685n145
Supporting Variantsnssv14100823
Samplessample409
Known GenesCBFA2T2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111812
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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