A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17464



Internal ID15828512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38868382..38868772hg38UCSC Ensembl
Outerchr9:38859978..38869113hg38UCSC Ensembl
Innerchr9:38868379..38868769hg19UCSC Ensembl
Outerchr9:38859975..38869110hg19UCSC Ensembl
Innerchr9:38858379..38858769hg18UCSC Ensembl
Outerchr9:38849975..38859110hg18UCSC Ensembl
Innerchr9:38858379..38858769hg17UCSC Ensembl
Outerchr9:38849975..38859110hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg389136
hg199136
hg189136
hg179136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA10839
Known Genes
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)nssv17464
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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