A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26284



Internal ID15495282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28099391..28099859hg38UCSC Ensembl
Outerchr16:28098773..28100383hg38UCSC Ensembl
Innerchr16:28110712..28111180hg19UCSC Ensembl
Outerchr16:28110094..28111704hg19UCSC Ensembl
Innerchr16:28018213..28018681hg18UCSC Ensembl
Outerchr16:28017595..28019205hg18UCSC Ensembl
Innerchr16:28018213..28018681hg17UCSC Ensembl
Outerchr16:28017595..28019205hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381611
hg191611
hg181611
hg171611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9408
Supporting Variants
SamplesNA19132
Known GenesXPO6
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)nssv26284
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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