A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566115



Internal ID16006838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104864865..104867202hg38UCSC Ensembl
Innerchr14:105331202..105333539hg19UCSC Ensembl
Innerchr14:104402247..104404584hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg382338
hg192338
hg182338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834675
Samples
Known GenesCEP170B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566115
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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