A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22284



Internal ID15840111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:29061415..29070229hg38UCSC Ensembl
Outerchr16:29059310..29073407hg38UCSC Ensembl
Innerchr16:29072736..29081550hg19UCSC Ensembl
Outerchr16:29070631..29084728hg19UCSC Ensembl
Innerchr16:28980237..28989051hg18UCSC Ensembl
Outerchr16:28978132..28992229hg18UCSC Ensembl
Innerchr16:28980237..28989051hg17UCSC Ensembl
Outerchr16:28978132..28992229hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3814098
hg1914098
hg1814098
hg1714098
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9422
Supporting Variants
SamplesNA18975
Known Genes
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)nssv22284
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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