A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5258n54



Internal ID18997434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83759413..83779689hg38UCSC Ensembl
chr16:83793018..83813294hg19UCSC Ensembl
chr16:82350519..82370795hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3820277
hg1920277
hg1820277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv573403, nsv573402
Samples
Known GenesCDH13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5258n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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