A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830868



Internal ID16108051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:168333086..168526732hg38UCSC Ensembl
Outerchr6:168733766..168927412hg19UCSC Ensembl
Outerchr6:168476615..168670261hg18UCSC Ensembl
Outerchr6:168552322..168745968hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38193647
hg19193647
hg18193647
hg17193647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1445813
Samples
Known GenesSMOC2
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)nsv830868
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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