A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974



Internal ID15839999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33799633..33803131hg38UCSC Ensembl
Outerchr9:33799220..33803575hg38UCSC Ensembl
Innerchr9:33799631..33803129hg19UCSC Ensembl
Outerchr9:33799218..33803573hg19UCSC Ensembl
Innerchr9:33789631..33793129hg18UCSC Ensembl
Outerchr9:33789218..33793573hg18UCSC Ensembl
Innerchr9:33789631..33793129hg17UCSC Ensembl
Outerchr9:33789218..33793573hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg384356
hg194356
hg184356
hg174356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8444
Supporting Variants
SamplesNA18975
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)nssv16974
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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