A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1448049



Internal ID16098653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:131495115..131647330hg38UCSC Ensembl
Outerchr9:134370502..134522717hg19UCSC Ensembl
Outerchr9:133360323..133512538hg18UCSC Ensembl
Outerchr9:131400056..131552271hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38152216
hg19152216
hg18152216
hg17152216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv831742
Supporting Variants
Samples
Known GenesPOMT1, PRRC2B, RAPGEF1, UCK1
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)nssv1448049
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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