A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2861n54



Internal ID18995037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111032912..111034977hg38UCSC Ensembl
chr12:111470716..111472781hg19UCSC Ensembl
chr12:109955099..109957164hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg382066
hg192066
hg182066
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560157, nsv560156
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2861n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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