A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140



Internal ID15490999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112749250..112750155hg38UCSC Ensembl
Outerchr9:112748119..112752039hg38UCSC Ensembl
Innerchr9:115511530..115512435hg19UCSC Ensembl
Outerchr9:115510399..115514319hg19UCSC Ensembl
Innerchr9:114551351..114552256hg18UCSC Ensembl
Outerchr9:114550220..114554140hg18UCSC Ensembl
Innerchr9:112591085..112591990hg17UCSC Ensembl
Outerchr9:112589954..112593874hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg383921
hg193921
hg183921
hg173921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8559
Supporting Variants
SamplesNA18853
Known GenesSNX30
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)nssv18140
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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