A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26368



Internal ID15495506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33097953..33098591hg38UCSC Ensembl
Outerchr16:33097365..33099852hg38UCSC Ensembl
Innerchr16:33109274..33109912hg19UCSC Ensembl
Outerchr16:33108686..33111173hg19UCSC Ensembl
Innerchr16:33016775..33017413hg18UCSC Ensembl
Outerchr16:33016187..33018674hg18UCSC Ensembl
Innerchr16:33016775..33017413hg17UCSC Ensembl
Outerchr16:33016187..33018674hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382488
hg192488
hg182488
hg172488
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA19132
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)nssv26368
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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