A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2899n54



Internal ID22770794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:117185846..117205262hg38UCSC Ensembl
chr12:117623651..117643067hg19UCSC Ensembl
chr12:116108034..116127450hg18UCSC Ensembl
Cytoband12q24.22
Allele length
AssemblyAllele length
hg3819417
hg1919417
hg1819417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv560347, nsv560346
Samples
Known GenesFBXO21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2899n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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