A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16241



Internal ID15485622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:41656870..41659463hg38UCSC Ensembl
Innerchr9:46126023..46128732hg19UCSC Ensembl
Outerchr9:46125616..46129884hg19UCSC Ensembl
Innerchr9:46016019..46018728hg18UCSC Ensembl
Outerchr9:46015612..46019880hg18UCSC Ensembl
Innerchr9:44678768..44681477hg17UCSC Ensembl
Outerchr9:44678361..44682629hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382594
hg194269
hg184269
hg174269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8474
Supporting Variants
SamplesNA12872
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)nssv16241
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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