A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154817



Internal ID22085322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:21394047..21415628hg38UCSC Ensembl
Outerchr12:21392422..21425337hg38UCSC Ensembl
Innerchr12:21546981..21568562hg19UCSC Ensembl
Outerchr12:21545356..21578271hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3832916
hg1932916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008958
Samples
Known GenesSLCO1A2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154817
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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