A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469511



Internal ID15534226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9608363..9752405hg38UCSC Ensembl
Innerchr4:9609987..9754029hg19UCSC Ensembl
Innerchr4:9219085..9363127hg18UCSC Ensembl
Innerchr4:9360870..9504912hg16UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38144043
hg19144043
hg18144043
hg16144043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673966
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)nsv469511
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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