A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10674



Internal ID15845637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:17495880..17799232hg38UCSC Ensembl
Outerchr5:17495989..17799341hg19UCSC Ensembl
Outerchr5:17548989..17835098hg18UCSC Ensembl
Outerchr5:17548989..17835098hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38303353
hg19303353
hg18286110
hg17286110
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14804, nssv14654, nssv13378, nssv13248, nssv12946, nssv15263, nssv12365, nssv13315, nssv12986, nssv13308, nssv13318, nssv13278, nssv13921, nssv14601, nssv13569, nssv12049, nssv13539, nssv13218, nssv13444, nssv12079, nssv12395, nssv13951, nssv14661, nssv13384, nssv12956, nssv14533, nssv14714, nssv14624, nssv13288, nssv14631, nssv13354, nssv12827, nssv12857, nssv13254, nssv13891, nssv13285, nssv12916, nssv14563, nssv13348, nssv13284, nssv14684, nssv13324, nssv15293
SamplesNA18980, NA18504, NA18563, NA18860, NA10839, NA18975, NA19007, NA10847, NA18572, NA18517, NA18564, NA19240, NA19144, NA12740, 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)nsv10674
Frequency
Sample Size31
Observed Gain8
Observed Loss12
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer