A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9477



Internal ID15500703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89569883..89608647hg38UCSC Ensembl
Outerchr16:89636291..89675055hg19UCSC Ensembl
Outerchr16:88163792..88202556hg18UCSC Ensembl
Outerchr16:88163792..88202556hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3838765
hg1938765
hg1838765
hg1738765
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28131, nssv26625, nssv26791, nssv22072, nssv25927, nssv23837, nssv23285, nssv24149, nssv22685, nssv25268, nssv24175, nssv26749, nssv22770
SamplesNA18517, NA07029, NA10863, NA12155, NA12740, NA07048, NA18502, NA18504, NA18942, NA19221, NA19132, NA18980
Known GenesCPNE7
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)nsv9477
Frequency
Sample Size31
Observed Gain11
Observed Loss1
Observed Complex0
Frequencyn/a


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