A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv56n97



Internal ID22815453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7811433..7985126hg38UCSC Ensembl
chr12:7964029..8137722hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38173694
hg19173694
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1154795, nsv1154794
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv56n97
Frequency
Sample Size131
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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