A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566138



Internal ID16006861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104874306..104884018hg38UCSC Ensembl
Innerchr14:105340643..105350355hg19UCSC Ensembl
Innerchr14:104411688..104421400hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg389713
hg199713
hg189713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834712
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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