A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10608



Internal ID15845571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:167886831..168074146hg38UCSC Ensembl
Outerchr4:168807982..168995297hg19UCSC Ensembl
Outerchr4:169044557..169231872hg18UCSC Ensembl
Outerchr4:169182712..169370027hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38187316
hg19187316
hg18187316
hg17187316
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11861, nssv13814, nssv12362, nssv12939, nssv12858, nssv11629, nssv13851, nssv12376, nssv12292, nssv12903, nssv13658, nssv13963, nssv13231, nssv12367, nssv12536, nssv13887, nssv12225, nssv12684, nssv12347, nssv14880, nssv14453, nssv12685, nssv12838, nssv12844, nssv13812, nssv13079, nssv11590, nssv12156, nssv12620, nssv11945
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA18942, NA07048, NA10839, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18537, NA18853, NA19132, NA18517, NA18564, NA19240, NA19144, NA12740, NA19173, NA18972, NA18552
Known Genes
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)nsv10608
Frequency
Sample Size31
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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