A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv565n145



Internal ID22813581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33374309..33375384hg38UCSC Ensembl
chr19:33865215..33866290hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110617, nsv3113126
Samplessample182, sample224, sample229
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv565n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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