A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18797



Internal ID15835803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64465382..64618864hg38UCSC Ensembl
Outerchr9:64464798..64620145hg38UCSC Ensembl
Innerchr9:69477800..69631282hg19UCSC Ensembl
Outerchr9:69477216..69632563hg19UCSC Ensembl
Innerchr9:68767620..68921102hg18UCSC Ensembl
Outerchr9:68767036..68922383hg18UCSC Ensembl
Innerchr9:67380676..67534158hg17UCSC Ensembl
Outerchr9:67380092..67535439hg17UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38155348
hg19155348
hg18155348
hg17155348
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8514
Supporting Variants
SamplesNA18563
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)nssv18797
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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