A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8852



Internal ID15846764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:86592457..86595746hg38UCSC Ensembl
Outerchr11:86303499..86306788hg19UCSC Ensembl
Outerchr11:85981147..85984436hg18UCSC Ensembl
Outerchr11:85981147..85984436hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383290
hg193290
hg183290
hg173290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv19374, nssv20265, nssv20056, nssv23167, nssv19916, nssv22866, nssv18499, nssv20948
SamplesNA18502, NA12155, NA18975, NA19007, NA18572, NA18537, NA19132, NA18552
Known GenesME3
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)nsv8852
Frequency
Sample Size31
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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