A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17913



Internal ID15828219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:29924398..29996259hg38UCSC Ensembl
Outerchr9:29922914..30003422hg38UCSC Ensembl
Innerchr9:29924396..29996257hg19UCSC Ensembl
Outerchr9:29922912..30003420hg19UCSC Ensembl
Innerchr9:29914396..29986257hg18UCSC Ensembl
Outerchr9:29912912..29993420hg18UCSC Ensembl
Innerchr9:29914396..29986257hg17UCSC 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 StatusS
Merged Variantsnsv8433
Supporting Variants
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)nssv17913
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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