A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834376



Internal ID16111559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:131426523..131595245hg38UCSC Ensembl
Outerchr2:132184096..132352818hg19UCSC Ensembl
Outerchr2:131900566..132069288hg18UCSC Ensembl
Outerchr2:132017828..132186550hg17UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38168723
hg19168723
hg18168723
hg17168723
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1442230, nssv1442231
Samples
Known GenesCCDC74A, LOC150776, LOC401010, MIR4784, MZT2A, RNU6-81P, TUBA3D
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)nsv834376
Frequency
Sample Size95
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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