A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv802023



Internal ID15749293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111034401..111038564hg38UCSC Ensembl
Innerchr12:111472205..111476368hg19UCSC Ensembl
Innerchr12:109956588..109960751hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg384164
hg194164
hg184164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560167
Supporting Variants
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv802023
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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