A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3966n54



Internal ID20137390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104864813..104865880hg38UCSC Ensembl
chr14:105331150..105332217hg19UCSC Ensembl
chr14:104402195..104403262hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg381068
hg191068
hg181068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566110, nsv566117, nsv566109
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3966n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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