A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16607



Internal ID15489132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:11988567..12321906hg17UCSC Ensembl
Outerchr8:11988287..12322453hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17334167
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8288
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)nssv16607
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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