A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17636



Internal ID15840975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:87771925..87773489hg38UCSC Ensembl
Outerchr9:87771119..87774285hg38UCSC Ensembl
Innerchr9:90386840..90388404hg19UCSC Ensembl
Outerchr9:90386034..90389200hg19UCSC Ensembl
Innerchr9:89576660..89578224hg18UCSC Ensembl
Outerchr9:89575854..89579020hg18UCSC Ensembl
Innerchr9:87616394..87617958hg17UCSC Ensembl
Outerchr9:87615588..87618754hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg383167
hg193167
hg183167
hg173167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8548
Supporting Variants
SamplesNA19007
Known GenesCTSL3P
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)nssv17636
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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