A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834185



Internal ID9425036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36230804..36392050hg38UCSC Ensembl
Outerchr22:36626850..36788095hg19UCSC Ensembl
Outerchr22:34956796..35118041hg18UCSC Ensembl
Outerchr22:34951350..35112595hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38161247
hg19161246
hg18161246
hg17161246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1456079
Samples
Known GenesAPOL1, APOL2, MIR6819, MYH9
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)nsv834185
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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