A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469764



Internal ID15534479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17721743..17880721hg38UCSC Ensembl
Innerchr5:17721852..17880830hg19UCSC Ensembl
Innerchr5:17757573..17916587hg18UCSC Ensembl
Innerchr5:17767317..17926331hg16UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38158979
hg19158979
hg18159015
hg16159015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675577
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)nsv469764
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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