A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831711



Internal ID16108894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:120503030..120705363hg38UCSC Ensembl
Outerchr9:123265308..123467641hg19UCSC Ensembl
Outerchr9:122305129..122507462hg18UCSC Ensembl
Outerchr9:120344862..120547195hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38202334
hg19202334
hg18202334
hg17202334
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1447987
Samples
Known GenesCDK5RAP2, MEGF9
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)nsv831711
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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