A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv566n145



Internal ID22813582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33792696..33801523hg38UCSC Ensembl
chr19:34283601..34292428hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg388828
hg198828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111284, nsv3113115
Samplessample81, sample296
Known GenesKCTD15
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv566n145
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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