A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9460



Internal ID15847372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75441791..75445652hg38UCSC Ensembl
Outerchr16:75475689..75479550hg19UCSC Ensembl
Outerchr16:74033190..74037051hg18UCSC Ensembl
Outerchr16:74033190..74037051hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg383862
hg193862
hg183862
hg173862
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv24378, nssv25138
SamplesNA12155, NA19173
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)nsv9460
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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