A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566137



Internal ID16006860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104865985..104893219hg38UCSC Ensembl
Innerchr14:105332322..105359556hg19UCSC Ensembl
Innerchr14:104403367..104430601hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3827235
hg1927235
hg1827235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834711
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566137
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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