A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115202



Internal ID21298468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:20721852..20848431hg38UCSC Ensembl
Innerchr12:20874786..21001365hg19UCSC Ensembl
Cytoband12p12.2
Allele length
AssemblyAllele length
hg38126580
hg19126580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14091565
Samplessample71
Known GenesSLCO1B3, SLCO1C1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115202
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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