A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469855



Internal ID15534570
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 StatusM
Merged Variants
Supporting Variantsnssv1676225, nssv1672781, nssv1674570, nssv1672615, nssv1676716, nssv1672571, nssv1672768, nssv1674686, nssv1676544, nssv1673786, nssv1673202, nssv1674226, nssv1673373, nssv1672512, nssv1673092, nssv1675161, nssv1676210, nssv1672904, nssv1673799
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)nsv469855
Frequency
Sample Size265
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer