A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469658



Internal ID15534373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:71859620..72008886hg38UCSC Ensembl
Innerchr18:69526856..69676121hg19UCSC Ensembl
Innerchr18:67677836..67827101hg18UCSC Ensembl
Innerchr18:67675825..67825090hg16UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38149267
hg19149266
hg18149266
hg16149266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675424
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)nsv469658
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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