A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5256n54



Internal ID20138680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83162159..83174417hg38UCSC Ensembl
chr16:83195764..83208022hg19UCSC Ensembl
chr16:81753265..81765523hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3812259
hg1912259
hg1812259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573392, nsv573391, nsv573393, nsv573389
Samples
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5256n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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