A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5313n54



Internal ID20138737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88795879..88806103hg38UCSC Ensembl
chr16:88862287..88872511hg19UCSC Ensembl
chr16:87389788..87400012hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3810225
hg1910225
hg1810225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573689, nsv573699, nsv573698
Samples
Known GenesCDT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5313n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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