A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1390n71



Internal ID6319010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:21352541..21426087hg19UCSC Ensembl
chr12:21243808..21317354hg18UCSC 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 Variantsnsv898885, nsv898888, nsv898887
SamplesIS39718, IS31044, IS35229, IS31546
Known GenesSLCO1A2, SLCO1B1
Method
Analysis
Platform
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)dgv1390n71
Frequency
Sample Size6533
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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