A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560161



Internal ID16000884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111034121..111043139hg38UCSC Ensembl
Innerchr12:111471925..111480943hg19UCSC Ensembl
Innerchr12:109956308..109965326hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg389019
hg199019
hg189019
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv802014
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560161
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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