A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv802012



Internal ID15749282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:111034121..111035030hg38UCSC Ensembl
Innerchr12:111471925..111472834hg19UCSC Ensembl
Innerchr12:109956308..109957217hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38910
hg19910
hg18910
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560160
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)nssv802012
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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