A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18557



Internal ID15835733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63100520..63124923hg38UCSC Ensembl
Outerchr9:63064927..63125331hg38UCSC Ensembl
Innerchr9:67005492..67029895hg19UCSC Ensembl
Outerchr9:66969899..67030303hg19UCSC Ensembl
Innerchr9:66745312..66769715hg18UCSC Ensembl
Outerchr9:66709719..66770123hg18UCSC Ensembl
Innerchr9:65575734..65600137hg17UCSC Ensembl
Outerchr9:65540141..65600545hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg3860405
hg1960405
hg1860405
hg1760405
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8497
Supporting Variants
SamplesNA18563
Known GenesLOC286297
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)nssv18557
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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