A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12014n54



Internal ID20145438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15543065..15555467hg38UCSC Ensembl
chr8:15400574..15412976hg19UCSC Ensembl
chr8:15444945..15457347hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3812403
hg1912403
hg1812403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610538, nsv610539, nsv610549, nsv610533, nsv610544, nsv610545
SamplesHGDP00157
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12014n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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