A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8783



Internal ID15846695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5738854..5747681hg38UCSC Ensembl
Outerchr11:5760084..5768911hg19UCSC Ensembl
Outerchr11:5716660..5725487hg18UCSC Ensembl
Outerchr11:5716660..5725487hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388828
hg198828
hg188828
hg178828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23273, nssv17710, nssv19640, nssv22021, nssv20587, nssv20319, nssv22677, nssv18049, nssv19536, nssv22003, nssv20588, nssv22272, nssv22544, nssv19915, nssv20818, nssv22790, nssv18185, nssv17891, nssv18984, nssv18902, nssv18052, nssv19516, nssv19496, nssv19833, nssv20009
SamplesNA18502, NA11830, NA18980, NA07029, NA18504, NA12155, NA12802, NA18860, NA18942, NA07048, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA18853, NA19132, NA18517, 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)nsv8783
Frequency
Sample Size31
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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