A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469618



Internal ID15187647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61845699..62023222hg38UCSC Ensembl
Innerchr9:42363622..42541100hg16UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38177524
hg16177479
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674917, nssv1675175, nssv1673120
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)nsv469618
Frequency
Sample Size265
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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