A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26577



Internal ID15486297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32771812..32772450hg38UCSC Ensembl
Outerchr16:32770551..32773033hg38UCSC Ensembl
Innerchr16:32783133..32783771hg19UCSC Ensembl
Outerchr16:32781872..32784354hg19UCSC Ensembl
Innerchr16:32690634..32691272hg18UCSC Ensembl
Outerchr16:32689373..32691855hg18UCSC Ensembl
Innerchr16:32690634..32691272hg17UCSC Ensembl
Outerchr16:32689373..32691855hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382483
hg192483
hg182483
hg172483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18502
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)nssv26577
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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