A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25063



Internal ID15483825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70116870..70164492hg38UCSC Ensembl
Outerchr16:70114032..70165401hg38UCSC Ensembl
Innerchr16:70150773..70198395hg19UCSC Ensembl
Outerchr16:70147935..70199304hg19UCSC Ensembl
Innerchr16:68708274..68755896hg18UCSC Ensembl
Outerchr16:68705436..68756805hg18UCSC Ensembl
Innerchr16:68708274..68755896hg17UCSC Ensembl
Outerchr16:68705436..68756805hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3851370
hg1951370
hg1851370
hg1751370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9455
Supporting Variants
SamplesNA12155
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)nssv25063
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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