A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051532



Internal ID19140751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:133042433..133123312hg38UCSC Ensembl
Innerchr12:133619019..133699898hg19UCSC Ensembl
Innerchr12:132129092..132209971hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3880880
hg1980880
hg1880880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1592n100
Supporting Variantsnssv3526393
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)nsv1051532
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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