A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469820



Internal ID15187849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10771224..10921664hg38UCSC Ensembl
Innerchr5:10771336..10921776hg19UCSC Ensembl
Innerchr5:10824336..10974776hg18UCSC Ensembl
Innerchr5:10824074..10974514hg16UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38150441
hg19150441
hg18150441
hg16150441
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675573, nssv1674725, nssv1673600, nssv1672592, nssv1675070, nssv1673090
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)nsv469820
Frequency
Sample Size265
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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