A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23633



Internal ID15488265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33964765..33966973hg38UCSC Ensembl
Outerchr16:33963477..33967799hg38UCSC Ensembl
Innerchr16:33767232..33769440hg19UCSC Ensembl
Outerchr16:33765944..33770266hg19UCSC Ensembl
Innerchr16:33674733..33676941hg18UCSC Ensembl
Outerchr16:33673445..33677767hg18UCSC Ensembl
Innerchr16:33674733..33676941hg17UCSC Ensembl
Outerchr16:33673445..33677767hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg384323
hg194323
hg184323
hg174323
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18537
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)nssv23633
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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