A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26698



Internal ID15491616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22373867..22374768hg38UCSC Ensembl
Outerchr16:22373335..22375533hg38UCSC Ensembl
Innerchr16:22385188..22386089hg19UCSC Ensembl
Outerchr16:22384656..22386854hg19UCSC Ensembl
Innerchr16:22292689..22293590hg18UCSC Ensembl
Outerchr16:22292157..22294355hg18UCSC Ensembl
Innerchr16:22292689..22293590hg17UCSC Ensembl
Outerchr16:22292157..22294355hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg382199
hg192199
hg182199
hg172199
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9404
Supporting Variants
SamplesNA18860
Known GenesCDR2
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)nssv26698
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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