A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv831673



Internal ID16455542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:102036902..102175994hg38UCSC Ensembl
Outerchr9:104799184..104938276hg19UCSC Ensembl
Outerchr9:103839005..103978097hg18UCSC Ensembl
Outerchr9:101878739..102017831hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38139093
hg19139093
hg18139093
hg17139093
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1447924, nssv1447926, nssv1447925
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)nsv831673
Frequency
Sample Size95
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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