A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469615



Internal ID15187644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22846234..22995927hg38UCSC Ensembl
Innerchr15:22877141..23026834hg19UCSC Ensembl
Innerchr15:20428582..20578275hg18UCSC Ensembl
Innerchr15:20424850..20574543hg16UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38149694
hg19149694
hg18149694
hg16149694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674061
Samples
Known GenesCYFIP1, NIPA2
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)nsv469615
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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