A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11809n54



Internal ID22779704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:452692..583699hg38UCSC Ensembl
chr8:402692..533699hg19UCSC Ensembl
chr8:392692..523699hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38131008
hg19131008
hg18131008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609456, nsv609455
SamplesHGDP00169
Known GenesFBXO25, TDRP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11809n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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