A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9484



Internal ID15847396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:90200541..90225276hg38UCSC Ensembl
Outerchr16:90266949..90291684hg19UCSC Ensembl
Outerchr16:88794450..88819185hg18UCSC Ensembl
Outerchr16:88794450..88819185hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3824736
hg1924736
hg1824736
hg1724736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24799, nssv23411
SamplesNA18563, NA19144
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)nsv9484
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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