A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv560163



Internal ID16000886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111034172..111035030hg38UCSC Ensembl
Innerchr12:111471976..111472834hg19UCSC Ensembl
Innerchr12:109956359..109957217hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38859
hg19859
hg18859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2864n54
Supporting Variantsnssv802016
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv560163
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer