A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615224



Internal ID16055947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114053497..114104774hg38UCSC Ensembl
Innerchr9:116815777..116867054hg19UCSC Ensembl
Innerchr9:115855598..115906875hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3851278
hg1951278
hg1851278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12855n54
Supporting Variantsnssv1176146, nssv1176462, nssv1176464, nssv1176460, nssv1176147, nssv1176463, nssv1176148, nssv1176461
SamplesHGDP00734, HGDP00617, HGDP00559, HGDP00582, HGDP00567, HGDP00606, HGDP00584, HGDP00573
Known GenesAMBP, KIF12, ZNF618
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615224
Frequency
Sample Size17421
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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