A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3972n54



Internal ID20137396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104865139..104874306hg38UCSC Ensembl
chr14:105331476..105340643hg19UCSC Ensembl
chr14:104402521..104411688hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg389168
hg199168
hg189168
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566131, nsv566134
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3972n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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