A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12017n54



Internal ID22779912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15545427..15568101hg38UCSC Ensembl
chr8:15402936..15425610hg19UCSC Ensembl
chr8:15447307..15469981hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3822675
hg1922675
hg1822675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610546, nsv610547, nsv610548
SamplesHGDP00805
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12017n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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