A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8433



Internal ID15846345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:29922914..30003422hg38UCSC Ensembl
Outerchr9:29922912..30003420hg19UCSC Ensembl
Outerchr9:29912912..29993420hg18UCSC Ensembl
Outerchr9:29912912..29993420hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3880509
hg1980509
hg1880509
hg1780509
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17913
SamplesNA07048
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)nsv8433
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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