A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25843



Internal ID15486866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72056256..72059062hg38UCSC Ensembl
Outerchr16:72055706..72059852hg38UCSC Ensembl
Innerchr16:72090155..72092961hg19UCSC Ensembl
Outerchr16:72089605..72093751hg19UCSC Ensembl
Innerchr16:70647656..70650462hg18UCSC Ensembl
Outerchr16:70647106..70651252hg18UCSC Ensembl
Innerchr16:70647656..70650462hg17UCSC Ensembl
Outerchr16:70647106..70651252hg17UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg384147
hg194147
hg184147
hg174147
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9456
Supporting Variants
SamplesNA18504
Known GenesHP
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)nssv25843
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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