A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20217



Internal ID15842102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38791174..38807291hg38UCSC Ensembl
Outerchr9:38790854..38808461hg38UCSC Ensembl
Innerchr9:38791171..38807288hg19UCSC Ensembl
Outerchr9:38790851..38808458hg19UCSC Ensembl
Innerchr9:38781171..38797288hg18UCSC Ensembl
Outerchr9:38780851..38798458hg18UCSC Ensembl
Innerchr9:38781171..38797288hg17UCSC Ensembl
Outerchr9:38780851..38798458hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3817608
hg1917608
hg1817608
hg1717608
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA19132
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)nssv20217
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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