A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv833679



Internal ID15780949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101006279..101245212hg38UCSC Ensembl
Innerchr14:101472616..101711549hg19UCSC Ensembl
Innerchr14:100542369..100781302hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38238934
hg19238934
hg18238934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565860
Supporting Variants
Samples
Known GenesMEG9, MIR1185-1, MIR1185-2, MIR1193, MIR1197, MIR134, MIR154, MIR299, MIR300, MIR323A, MIR323B, MIR329-1, MIR329-2, MIR369, MIR376A1, MIR376A2, MIR376B, MIR376C, MIR377, MIR379, MIR380, MIR381, MIR381HG, MIR382, MIR409, MIR410, MIR411, MIR412, MIR485, MIR487A, MIR487B, MIR494, MIR495, MIR496, MIR539, MIR541, MIR543, MIR654, MIR655, MIR656, MIR668, MIR758, MIR889
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv833679
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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