A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1592n100



Internal ID22787679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:133024370..133123312hg38UCSC Ensembl
chr12:133600956..133699898hg19UCSC Ensembl
chr12:132111029..132209971hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3898943
hg1998943
hg1898943
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051532, nsv1041298, nsv1045005
Samples
Known GenesZNF140, ZNF84, ZNF891
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1592n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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