A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20841



Internal ID15838574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62108854..62109791hg38UCSC Ensembl
Outerchr9:62102643..62110108hg38UCSC Ensembl
Innerchr9:67546365..67547302hg19UCSC Ensembl
Outerchr9:67546048..67553513hg19UCSC Ensembl
Innerchr9:67136185..67137122hg18UCSC Ensembl
Outerchr9:67135868..67143333hg18UCSC Ensembl
Innerchr9:66036523..66037460hg17UCSC Ensembl
Outerchr9:66036206..66043672hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg387466
hg197466
hg187466
hg177467
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8499
Supporting Variants
SamplesNA18860
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)nssv20841
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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