A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834686



Internal ID16111869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:49068614..49233123hg38UCSC Ensembl
Outerchr3:49106047..49270556hg19UCSC Ensembl
Outerchr3:49081051..49245560hg18UCSC Ensembl
Outerchr3:49081051..49245560hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38164510
hg19164510
hg18164510
hg17164510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1442786
Samples
Known GenesC3orf84, CCDC36, CCDC71, KLHDC8B, LAMB2, LAMB2P1, MIR6890, QARS, QRICH1, USP19
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)nsv834686
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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