A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2862n54



Internal ID18995038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111034121..111034717hg38UCSC Ensembl
chr12:111471925..111472521hg19UCSC Ensembl
chr12:109956308..109956904hg18UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38597
hg19597
hg18597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560158, nsv560162
Samples
Known GenesCUX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2862n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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