A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833418



Internal ID16457287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:33222579..33363494hg38UCSC Ensembl
Outerchr17:31549597..31690512hg19UCSC Ensembl
Outerchr17:28573710..28714625hg18UCSC Ensembl
Outerchr17:28573710..28714625hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38140916
hg19140916
hg18140916
hg17140916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1453255
Samples
Known GenesASIC2
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)nsv833418
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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