A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8425n54



Internal ID22776320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85868139..85995074hg38UCSC Ensembl
chr3:85917289..86044224hg19UCSC Ensembl
chr3:85999979..86126914hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38126936
hg19126936
hg18126936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590912, nsv590913
Samples1782681169_A, 1780854061_A
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8425n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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