A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv685n145



Internal ID22813701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33588592..33596189hg38UCSC Ensembl
chr20:32176398..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 Variants
Supporting Variantsnsv3111812, nsv3110299
Samplessample350, sample409
Known GenesCBFA2T2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv685n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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