A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712692



Internal ID19010973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:133106281..133183162hg38UCSC Ensembl
Innerchr12:133682867..133759748hg19UCSC Ensembl
Innerchr12:132192940..132269821hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3876882
hg1976882
hg1876882
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047733
Supporting Variants
Samples
Known GenesZNF10, ZNF140, ZNF268, ZNF891
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712692
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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