A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv830558



Internal ID16107741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:179197390..179378603hg38UCSC Ensembl
Outerchr5:178624391..178805604hg19UCSC Ensembl
Outerchr5:178556997..178738210hg18UCSC Ensembl
Outerchr5:178556997..178738210hg17UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38181214
hg19181214
hg18181214
hg17181214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1445157
Samples
Known GenesADAMTS2
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)nsv830558
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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