A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469535



Internal ID15534250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41629654..41736086hg38UCSC Ensembl
Innerchr9:46298863..46405393hg19UCSC Ensembl
Innerchr9:46188859..46295389hg18UCSC Ensembl
Innerchr9:43564561..43671091hg16UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38106433
hg19106531
hg18106531
hg16106531
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673498, nssv1673039
Samples
Known GenesFAM27E1
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)nsv469535
Frequency
Sample Size265
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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