A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22584



Internal ID15493613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70111551..70172291hg38UCSC Ensembl
Outerchr16:70110189..70173094hg38UCSC Ensembl
Innerchr16:70145454..70206194hg19UCSC Ensembl
Outerchr16:70144092..70206997hg19UCSC Ensembl
Innerchr16:68702955..68763695hg18UCSC Ensembl
Outerchr16:68701593..68764498hg18UCSC Ensembl
Innerchr16:68702955..68763695hg17UCSC Ensembl
Outerchr16:68701593..68764498hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3862906
hg1962906
hg1862906
hg1762906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9455
Supporting Variants
SamplesNA18975
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)nssv22584
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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