A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115499



Internal ID21298765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:61391022..61501404hg38UCSC Ensembl
Innerchr12:61784803..61895185hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38110383
hg19110383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14092610
Samplessample303
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115499
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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