A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22536



Internal ID15829597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55761922..55788975hg38UCSC Ensembl
Outerchr16:55760408..55789680hg38UCSC Ensembl
Innerchr16:55795834..55822887hg19UCSC Ensembl
Outerchr16:55794320..55823592hg19UCSC Ensembl
Innerchr16:54353335..54380388hg18UCSC Ensembl
Outerchr16:54351821..54381093hg18UCSC Ensembl
Innerchr16:54353335..54380388hg17UCSC Ensembl
Outerchr16:54351821..54381093hg17UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3829273
hg1929273
hg1829273
hg1729273
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9445
Supporting Variants
SamplesNA10863
Known GenesCES1P1
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)nssv22536
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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