A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9410



Internal ID15847322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28199300..28210286hg38UCSC Ensembl
Outerchr16:28210621..28221607hg19UCSC Ensembl
Outerchr16:28118122..28129108hg18UCSC Ensembl
Outerchr16:28118122..28129108hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810987
hg1910987
hg1810987
hg1710987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv21996, nssv23787
SamplesNA10863, NA19173
Known GenesXPO6
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)nsv9410
Frequency
Sample Size31
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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