A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830863



Internal ID16454732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:165389975..165556603hg38UCSC Ensembl
Outerchr6:165803464..165970091hg19UCSC Ensembl
Outerchr6:165723454..165890081hg18UCSC Ensembl
Outerchr6:165773875..165940502hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38166629
hg19166628
hg18166628
hg17166628
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1445807
Samples
Known GenesPDE10A
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)nsv830863
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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