A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26736



Internal ID15486171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70120507..70156202hg38UCSC Ensembl
Outerchr16:70118898..70157003hg38UCSC Ensembl
Innerchr16:70154410..70190105hg19UCSC Ensembl
Outerchr16:70152801..70190906hg19UCSC Ensembl
Innerchr16:68711911..68747606hg18UCSC Ensembl
Outerchr16:68710302..68748407hg18UCSC Ensembl
Innerchr16:68711911..68747606hg17UCSC Ensembl
Outerchr16:68710302..68748407hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3838106
hg1938106
hg1838106
hg1738106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9455
Supporting Variants
SamplesNA18502
Known GenesPDPR
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)nssv26736
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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