A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10658



Internal ID15845621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:3592072..3608510hg38UCSC Ensembl
Outerchr5:3592186..3608624hg19UCSC Ensembl
Outerchr5:3645186..3661624hg18UCSC Ensembl
Outerchr5:3645186..3661624hg17UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3816439
hg1916439
hg1816439
hg1716439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15300
SamplesNA19221
Known GenesIRX1
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv10658
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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