A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3133n54



Internal ID22771028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:43167710..43214041hg38UCSC Ensembl
chr13:43741846..43788177hg19UCSC Ensembl
chr13:42639846..42686177hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3846332
hg1946332
hg1846332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561571, nsv561570, nsv561572
Samples
Known GenesENOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3133n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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