A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9483



Internal ID15847395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:90095961..90125699hg38UCSC Ensembl
Outerchr16:90162369..90192107hg19UCSC Ensembl
Outerchr16:88689870..88719608hg18UCSC Ensembl
Outerchr16:88689870..88719608hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3829739
hg1929739
hg1829739
hg1729739
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25318, nssv23864, nssv24508, nssv26760, nssv23865, nssv22773, nssv23160, nssv26802, nssv23353, nssv20809, nssv26638, nssv22703, nssv20705
SamplesNA18502, NA18980, NA12155, NA18563, NA18975, NA19007, NA10847, NA10863, NA18572, NA18853, NA19132, NA18517, 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)nsv9483
Frequency
Sample Size31
Observed Gain4
Observed Loss9
Observed Complex0
Frequencyn/a


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