A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv829688



Internal ID16106871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:117954927..118123511hg38UCSC Ensembl
Outerchr3:117673774..117842358hg19UCSC Ensembl
Outerchr3:119156464..119325048hg18UCSC Ensembl
Outerchr3:119156464..119325048hg17UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38168585
hg19168585
hg18168585
hg17168585
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1443025
Samples
Known Genes
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)nsv829688
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer