A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8559



Internal ID15499785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:112748119..112752039hg38UCSC Ensembl
Outerchr9:115510399..115514319hg19UCSC Ensembl
Outerchr9:114550220..114554140hg18UCSC 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 StatusM
Merged Variants
Supporting Variantsnssv18140, nssv18256
SamplesNA18552, NA18853
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)nsv8559
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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