A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv833058



Internal ID16110241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:76943554..77101298hg38UCSC Ensembl
Outerchr15:77235895..77393640hg19UCSC Ensembl
Outerchr15:75022950..75180695hg18UCSC Ensembl
Outerchr15:75022950..75180695hg17UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38157745
hg19157746
hg18157746
hg17157746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1452035, nssv1452025, nssv1452033, nssv1452034, nssv1452030, nssv1452032, nssv1452027, nssv1452029, nssv1452031, nssv1452028, nssv1452026
Samples
Known GenesPSTPIP1, RCN2, TSPAN3
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)nsv833058
Frequency
Sample Size95
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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