A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14091565



Internal ID21291292
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 StatusS
Merged Variantsnsv3115202
Supporting Variants
Samplessample71
Known GenesSLCO1B3, SLCO1C1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14091565
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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