A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469893



Internal ID15534608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17603979..17803134hg38UCSC Ensembl
Innerchr5:17604088..17803243hg19UCSC Ensembl
Innerchr5:17647192..17839000hg18UCSC Ensembl
Innerchr5:17656936..17848744hg16UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38199156
hg19199156
hg18191809
hg16191809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675661
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)nsv469893
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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