A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26241



Internal ID15487667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32049436..32051468hg38UCSC Ensembl
Outerchr16:32048805..32052244hg38UCSC Ensembl
Innerchr16:32060757..32062789hg19UCSC Ensembl
Outerchr16:32060126..32063565hg19UCSC Ensembl
Innerchr16:31968258..31970290hg18UCSC Ensembl
Outerchr16:31967627..31971066hg18UCSC Ensembl
Innerchr16:31968258..31970290hg17UCSC Ensembl
Outerchr16:31967627..31971066hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383440
hg193440
hg183440
hg173440
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18517
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)nssv26241
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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