A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469685



Internal ID15187714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34438970..34590429hg38UCSC Ensembl
Innerchr15:34731171..34882630hg19UCSC Ensembl
Innerchr15:32518463..32669922hg18UCSC Ensembl
Innerchr15:32447227..32598686hg16UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38151460
hg19151460
hg18151460
hg16151460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672286, nssv1674461, nssv1673122, nssv1675086, nssv1673570
Samples
Known GenesGOLGA8B, MIR1233-1, MIR1233-2
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)nsv469685
Frequency
Sample Size265
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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