A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566136



Internal ID16006859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104865556..104881702hg38UCSC Ensembl
Innerchr14:105331893..105348039hg19UCSC Ensembl
Innerchr14:104402938..104419084hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3816147
hg1916147
hg1816147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3971n54
Supporting Variantsnssv834710
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566136
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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