A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3060n54



Internal ID22770955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133104113..133202210hg38UCSC Ensembl
chr12:133680699..133778796hg19UCSC Ensembl
chr12:132190772..132288869hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3898098
hg1998098
hg1898098
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561146, nsv561147
Samples1780862379_A
Known GenesZNF10, ZNF140, ZNF268, ZNF891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3060n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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