A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24225



Internal ID15483637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33805417..33813616hg38UCSC Ensembl
Outerchr16:33804088..33815003hg38UCSC Ensembl
Innerchr16:33607884..33616083hg19UCSC Ensembl
Outerchr16:33606555..33617470hg19UCSC Ensembl
Innerchr16:33515385..33523584hg18UCSC Ensembl
Outerchr16:33514056..33524971hg18UCSC Ensembl
Innerchr16:33515385..33523584hg17UCSC Ensembl
Outerchr16:33514056..33524971hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810916
hg1910916
hg1810916
hg1710916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA11830
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)nssv24225
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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