A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3766n54



Internal ID20137190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73532494..73559754hg38UCSC Ensembl
chr14:73999198..74026458hg19UCSC Ensembl
chr14:73068951..73096211hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3827261
hg1927261
hg1827261
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565132, nsv565126, nsv565128, nsv565145, nsv565127
Samples
Known GenesACOT1, HEATR4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3766n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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