A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17887



Internal ID15830244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67061971..67216417hg38UCSC Ensembl
Outerchr9:67061209..67216978hg38UCSC Ensembl
Innerchr9:40476424..40630870hg19UCSC Ensembl
Outerchr9:40475863..40631632hg19UCSC Ensembl
Innerchr9:40466424..40620870hg18UCSC Ensembl
Outerchr9:40465863..40621632hg18UCSC Ensembl
Innerchr9:40205707..40360153hg17UCSC Ensembl
Outerchr9:40205146..40360915hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38155770
hg19155770
hg18155770
hg17155770
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8456
Supporting Variants
SamplesNA11830
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)nssv17887
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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