A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560156



Internal ID16000879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111032912..111034717hg38UCSC Ensembl
Innerchr12:111470716..111472521hg19UCSC Ensembl
Innerchr12:109955099..109956904hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381806
hg191806
hg181806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2861n54
Supporting Variantsnssv802004
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560156
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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