A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26738



Internal ID15487434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:87882332..87890371hg38UCSC Ensembl
Outerchr16:87881137..87891135hg38UCSC Ensembl
Innerchr16:87915938..87923977hg19UCSC Ensembl
Outerchr16:87914743..87924741hg19UCSC Ensembl
Innerchr16:86473439..86481478hg18UCSC Ensembl
Outerchr16:86472244..86482242hg18UCSC Ensembl
Innerchr16:86473439..86481478hg17UCSC Ensembl
Outerchr16:86472244..86482242hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg389999
hg199999
hg189999
hg179999
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9471
Supporting Variants
SamplesNA18517
Known GenesCA5A
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)nssv26738
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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