A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11585



Internal ID15482475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:68507752..68670645hg38UCSC Ensembl
Outerchr4:68507471..68670928hg38UCSC Ensembl
Innerchr4:69373470..69536363hg19UCSC Ensembl
Outerchr4:69373189..69536646hg19UCSC Ensembl
Innerchr4:69056065..69218958hg18UCSC Ensembl
Outerchr4:69055784..69219241hg18UCSC Ensembl
Innerchr4:69202236..69365129hg17UCSC Ensembl
Outerchr4:69201955..69365412hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38163458
hg19163458
hg18163458
hg17163458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10516
Supporting Variants
SamplesNA10847
Known GenesUGT2B15, UGT2B17
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)nssv11585
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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