A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1450482



Internal ID16101086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110447888..110643646hg38UCSC Ensembl
Outerchr13:111100235..111295993hg19UCSC Ensembl
Outerchr13:109898236..110093994hg18UCSC Ensembl
Outerchr13:109898236..110093994hg17UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38195759
hg19195759
hg18195759
hg17195759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv832720
Supporting Variants
Samples
Known GenesCARKD, CARS2, COL4A2, COL4A2-AS1, RAB20
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)nssv1450482
Frequency
Sample Size95
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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