A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469784



Internal ID15187813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63596968..63776777hg38UCSC Ensembl
Innerchr9:68192702..68372511hg19UCSC Ensembl
Innerchr9:67682522..67862331hg18UCSC Ensembl
Innerchr9:64860432..65060890hg16UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38179810
hg19179810
hg18179810
hg16200459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675374
Samples
Known Genes
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)nsv469784
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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