A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8422n54



Internal ID22776317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85109582..85215861hg38UCSC Ensembl
chr3:85158733..85265011hg19UCSC Ensembl
chr3:85241423..85347701hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38106280
hg19106279
hg18106279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590900, nsv590898
Samples
Known GenesCADM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8422n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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