A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1443045



Internal ID16440335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:121326946..121509128hg38UCSC Ensembl
Outerchr3:121045793..121227975hg19UCSC Ensembl
Outerchr3:122528483..122710665hg18UCSC Ensembl
Outerchr3:122528483..122710665hg17UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38182183
hg19182183
hg18182183
hg17182183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv829702
Supporting Variants
Samples
Known GenesPOLQ, STXBP5L
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)nssv1443045
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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