A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17575



Internal ID15840467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33799633..33807113hg38UCSC Ensembl
Outerchr9:33799220..33807433hg38UCSC Ensembl
Innerchr9:33799631..33807111hg19UCSC Ensembl
Outerchr9:33799218..33807431hg19UCSC Ensembl
Innerchr9:33789631..33797111hg18UCSC Ensembl
Outerchr9:33789218..33797431hg18UCSC Ensembl
Innerchr9:33789631..33797111hg17UCSC Ensembl
Outerchr9:33789218..33797431hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg388214
hg198214
hg188214
hg178214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8444
Supporting Variants
SamplesNA18980
Known GenesPRSS3
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)nssv17575
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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