A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2842n54



Internal ID22770737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:106240944..106248444hg38UCSC Ensembl
chr12:106634722..106642222hg19UCSC Ensembl
chr12:105158852..105166352hg18UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg387501
hg197501
hg187501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560058, nsv560057, nsv560056
Samples
Known GenesCKAP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2842n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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