A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv805966



Internal ID16099922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:133104113..133157527hg38UCSC Ensembl
Innerchr12:133680699..133734113hg19UCSC Ensembl
Innerchr12:132190772..132244186hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3853415
hg1953415
hg1853415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv561145
Supporting Variants
Samples
Known GenesZNF10, ZNF140, ZNF891
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv805966
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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