A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv834227



Internal ID16458096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:46499528..46743584hg38UCSC Ensembl
Outerchr22:46895425..47139481hg19UCSC Ensembl
Outerchr22:45274089..45518145hg18UCSC Ensembl
Outerchr22:45215944..45460000hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38244057
hg19244057
hg18244057
hg17244057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1456183, nssv1456182, nssv1456179, nssv1456178, nssv1456181, nssv1456184, nssv1456180
Samples
Known GenesCELSR1, CERK, GRAMD4
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)nsv834227
Frequency
Sample Size95
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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