A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18499



Internal ID15837151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86593564..86595101hg38UCSC Ensembl
Outerchr11:86592457..86595746hg38UCSC Ensembl
Innerchr11:86304606..86306143hg19UCSC Ensembl
Outerchr11:86303499..86306788hg19UCSC Ensembl
Innerchr11:85982254..85983791hg18UCSC Ensembl
Outerchr11:85981147..85984436hg18UCSC Ensembl
Innerchr11:85982254..85983791hg17UCSC 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 StatusS
Merged Variantsnsv8852
Supporting Variants
SamplesNA18572
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)nssv18499
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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