A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469665



Internal ID15534380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65166987..65325103hg38UCSC Ensembl
Innerchr9:70060587..70469616hg19UCSC Ensembl
Innerchr9:69350407..69709436hg18UCSC Ensembl
Innerchr9:66047380..66205668hg16UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38158117
hg19409030
hg18359030
hg16158289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675806
Samples
Known GenesCBWD3, CBWD5, FOXD4L2, FOXD4L4, FOXD4L5
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)nsv469665
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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