A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12015n54



Internal ID20145439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15544498..15551464hg38UCSC Ensembl
chr8:15402007..15408973hg19UCSC Ensembl
chr8:15446378..15453344hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg386967
hg196967
hg186967
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610534, nsv610536, nsv610540, nsv610542, nsv610541, nsv610535
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12015n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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