A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9467



Internal ID15847379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85970029..85976673hg38UCSC Ensembl
Outerchr16:86003635..86010279hg19UCSC Ensembl
Outerchr16:84561136..84567780hg18UCSC Ensembl
Outerchr16:84561136..84567780hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg386645
hg196645
hg186645
hg176645
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23297, nssv24456, nssv23201, nssv20680, nssv20615, nssv25560, nssv26511, nssv21251, nssv24541, nssv26599, nssv23662, nssv22626, nssv23811, nssv26685, nssv28125, nssv24042, nssv27103, nssv23132, nssv20719, nssv22674, nssv23524, nssv21982
SamplesNA11830, NA18563, NA12802, NA18860, NA18942, NA07048, NA18975, NA19007, NA10847, NA10863, NA12872, NA18572, NA19221, NA18853, NA19132, NA18517, NA18564, NA19240, NA12740, NA19173, NA18972, NA18552
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)nsv9467
Frequency
Sample Size31
Observed Gain21
Observed Loss1
Observed Complex0
Frequencyn/a


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