A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19178



Internal ID15830860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:66064380..66070586hg38UCSC Ensembl
Outerchr9:66055289..66082375hg38UCSC Ensembl
Innerchr9:43044958..43051164hg19UCSC Ensembl
Outerchr9:43035867..43062953hg19UCSC Ensembl
Innerchr9:45075542..45081748hg17UCSC Ensembl
Outerchr9:45066451..45093537hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3827087
hg1927087
hg1727087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8479
Supporting Variants
SamplesNA12155
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)nssv19178
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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