A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10751



Internal ID15845714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:138470006..138485327hg38UCSC Ensembl
Outerchr5:137805695..137821016hg19UCSC Ensembl
Outerchr5:137833594..137848915hg18UCSC Ensembl
Outerchr5:137833594..137848915hg17UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3815322
hg1915322
hg1815322
hg1715322
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13397, nssv13282, nssv14223, nssv12940, nssv14982, nssv16133, nssv14829, nssv13734, nssv14219, nssv13592, nssv15373, nssv15343, nssv14164, nssv15597, nssv14641, nssv15561, nssv13665, nssv14166, nssv13715, nssv16140, nssv13496, nssv12671, nssv12529, nssv13585, nssv14116, nssv13700, nssv13908, nssv14678, nssv13717, nssv13918, nssv15734
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)nsv10751
Frequency
Sample Size31
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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