A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113296



Internal ID21296562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3898439..3977173hg38UCSC Ensembl
Innerchr16:3948440..4027174hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3878735
hg1978735
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14098344
Samplessample71
Known GenesADCY9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113296
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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