A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv563n145



Internal ID22813579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33371984..33376385hg38UCSC Ensembl
chr19:33862890..33867291hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384402
hg194402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117830, nsv3116344
Samplessample70, sample220, sample11, sample188
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv563n145
Frequency
Sample Size467
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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