A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8540



Internal ID15499766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:83843672..83855454hg38UCSC Ensembl
Outerchr9:86458587..86470369hg19UCSC Ensembl
Outerchr9:85648407..85660189hg18UCSC Ensembl
Outerchr9:83688141..83699923hg17UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3811783
hg1911783
hg1811783
hg1711783
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16361
SamplesNA12872
Known GenesKIF27
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)nsv8540
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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