A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112862



Internal ID21296128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:33752787..34089444hg38UCSC Ensembl
Innerchr16:33555254..33891911hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38336658
hg19336658
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv437n145
Supporting Variantsnssv14098388
Samplessample95
Known GenesRNU6-76P
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112862
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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