A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3768n54



Internal ID20137192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73533785..73539789hg38UCSC Ensembl
chr14:74000489..74006493hg19UCSC Ensembl
chr14:73070242..73076246hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg386005
hg196005
hg186005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565135, nsv565134
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3768n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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