A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26838



Internal ID15491718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32562515..32634229hg38UCSC Ensembl
Outerchr16:32481626..32634608hg38UCSC Ensembl
Innerchr16:32573836..32645550hg19UCSC Ensembl
Outerchr16:32492947..32645929hg19UCSC Ensembl
Innerchr16:32481337..32553051hg18UCSC Ensembl
Outerchr16:32400448..32553430hg18UCSC Ensembl
Innerchr16:32481337..32553051hg17UCSC Ensembl
Outerchr16:32400448..32553430hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38152983
hg19152983
hg18152983
hg17152983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18860
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)nssv26838
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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