A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469516



Internal ID15534231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:28699895..28849355hg38UCSC Ensembl
Innerchr11:28721442..28870902hg19UCSC Ensembl
Innerchr11:28678018..28827478hg18UCSC Ensembl
Innerchr11:28685751..28835211hg16UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38149461
hg19149461
hg18149461
hg16149461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674821
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)nsv469516
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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