A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26159



Internal ID15493007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32187773..32188214hg38UCSC Ensembl
Outerchr16:32187314..32189247hg38UCSC Ensembl
Innerchr16:32199094..32199535hg19UCSC Ensembl
Outerchr16:32198635..32200568hg19UCSC Ensembl
Innerchr16:32106595..32107036hg18UCSC Ensembl
Outerchr16:32106136..32108069hg18UCSC Ensembl
Innerchr16:32106595..32107036hg17UCSC Ensembl
Outerchr16:32106136..32108069hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381934
hg191934
hg181934
hg171934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA18972
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)nssv26159
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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