A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116899



Internal ID21300165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33752787..34123075hg38UCSC Ensembl
Innerchr16:33555254..33925542hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38370289
hg19370289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv437n145
Supporting Variantsnssv14098287
Samplessample46
Known GenesRNU6-76P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116899
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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