A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22816



Internal ID15491128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32696139..32750435hg38UCSC Ensembl
Outerchr16:32696075..32750502hg38UCSC Ensembl
Innerchr16:32707460..32761756hg19UCSC Ensembl
Outerchr16:32707396..32761823hg19UCSC Ensembl
Innerchr16:32614961..32669257hg18UCSC Ensembl
Outerchr16:32614897..32669324hg18UCSC Ensembl
Innerchr16:32614961..32669257hg17UCSC Ensembl
Outerchr16:32614897..32669324hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3854428
hg1954428
hg1854428
hg1754428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18853
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)nssv22816
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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