A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3971n54



Internal ID20137395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104865033..104881702hg38UCSC Ensembl
chr14:105331370..105348039hg19UCSC Ensembl
chr14:104402415..104419084hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3816670
hg1916670
hg1816670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv566132, nsv566136, nsv566123
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3971n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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