A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv564n145



Internal ID22813580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33372902..33377047hg38UCSC Ensembl
chr19:33863808..33867953hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384146
hg194146
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117790, nsv3115099, nsv3115262, nsv3116409
Samplessample306, sample373, sample171, sample158, sample372, sample309, sample162
Known GenesCEBPG
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv564n145
Frequency
Sample Size467
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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