A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1451874



Internal ID16102478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:34543795..34708959hg38UCSC Ensembl
Outerchr15:34835996..35001160hg19UCSC Ensembl
Outerchr15:32623288..32788452hg18UCSC Ensembl
Outerchr15:32623288..32788452hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38165165
hg19165165
hg18165165
hg17165165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv832965
Supporting Variants
Samples
Known GenesGOLGA8B, MIR5588
MethodBAC aCGH
AnalysisExperimental SDs (SDautosome) were calculated for each experiment on the basis of the log2 ratios of the 24,392 reliable clones minus the clones removed because of low signal-to-noise ratio (SNR) or high SD of replicate clone measures (SDclone). Thresholds for determining CNV clones were set at a multiple of the SDautosome value. For each experiment, clones were annotated as uninformative if they were filtered via SNR or SDclone, as a CNV loss if the log2 ratio was less than the negative threshold, as unchanged if the log2 ratio was between the negative and positive thresholds, and as a CNV gain if the log2 ratio was above the positive threshold.
PlatformGPL2616
Comments
ReferenceWong_et_al_2007
Pubmed ID17160897
Accession Number(s)nssv1451874
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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