A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1444492



Internal ID16095096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:55673052..55846654hg38UCSC Ensembl
Outerchr5:54968880..55142482hg19UCSC Ensembl
Outerchr5:55004637..55178239hg18UCSC Ensembl
Outerchr5:55004637..55178239hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38173603
hg19173603
hg18173603
hg17173603
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv830306
Supporting Variants
Samples
Known GenesDDX4, SLC38A9
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)nssv1444492
Frequency
Sample Size95
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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