A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8795



Internal ID15846707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:18919677..18950763hg38UCSC Ensembl
Outerchr11:18941224..18972310hg19UCSC Ensembl
Outerchr11:18897800..18928886hg18UCSC Ensembl
Outerchr11:18897800..18928886hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3831087
hg1931087
hg1831087
hg1731087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25131, nssv19935, nssv19656, nssv20065, nssv20439, nssv20267, nssv22362, nssv19790, nssv18992, nssv18275, nssv19134, nssv20678, nssv19924, nssv17920, nssv18229, nssv22201, nssv18041, nssv19636, nssv22153, nssv19586, nssv18202, nssv20159, nssv23443, nssv19938, nssv22634, nssv22935, nssv22794, nssv19953, nssv20707, nssv20908
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 GenesMRGPRX1
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)nsv8795
Frequency
Sample Size31
Observed Gain30
Observed Loss0
Observed Complex0
Frequencyn/a


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