A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113871



Internal ID21297137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31551189..31624079hg38UCSC Ensembl
Innerchr16:31562510..31635400hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3872891
hg1972891
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14099213
Samplessample188
Known GenesYBX3P1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113871
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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