A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1674686



Internal ID15532194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19902981..20036861hg38UCSC Ensembl
Innerchr14:20371140..20505020hg19UCSC Ensembl
Innerchr14:19440980..19574860hg18UCSC Ensembl
Innerchr14:18361268..18495148hg16UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38133881
hg19133881
hg18133881
hg16133881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469855
Supporting Variants
Samples
Known GenesOR4K1, OR4K13, OR4K14, OR4K15, OR4K5
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nssv1674686
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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