A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1452086



Internal ID16102690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:90996315..91056472hg38UCSC Ensembl
Outerchr15:91539545..91599702hg19UCSC Ensembl
Outerchr15:89340549..89400706hg18UCSC Ensembl
Outerchr15:89340549..89400706hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3860158
hg1960158
hg1860158
hg1760158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv833091
Supporting Variants
Samples
Known GenesVPS33B
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)nssv1452086
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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