A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1389n71



Internal ID6319009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21294293..21321482hg19UCSC Ensembl
chr12:21185560..21212749hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv898882, nsv898881
SamplesIS30532, MS18978, MS12209
Known GenesSLCO1B1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1389n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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