A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26451



Internal ID15487562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33349103..33349106hg38UCSC Ensembl
Outerchr16:33348225..33349168hg38UCSC Ensembl
Innerchr16:33250344..33250347hg19UCSC Ensembl
Outerchr16:33249466..33250409hg19UCSC Ensembl
Innerchr16:33157845..33157848hg18UCSC Ensembl
Outerchr16:33156967..33157910hg18UCSC Ensembl
Innerchr16:33157845..33157848hg17UCSC Ensembl
Outerchr16:33156967..33157910hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38944
hg19944
hg18944
hg17944
Variant TypeCNV loss
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)nssv26451
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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