A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469595



Internal ID15534310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:71166185..71333967hg38UCSC Ensembl
Innerchr15:71458524..71626306hg19UCSC Ensembl
Innerchr15:69245578..69413360hg18UCSC Ensembl
Innerchr15:69174342..69342124hg16UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38167783
hg19167783
hg18167783
hg16167783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673572, nssv1676347, nssv1674468, nssv1675616, nssv1675164, nssv1672536, nssv1672408, nssv1675167, nssv1675222, nssv1672413, nssv1675736, nssv1673820, nssv1676196, nssv1676044, nssv1674284, nssv1676248
Samples
Known GenesTHSD4
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)nsv469595
Frequency
Sample Size265
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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