A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3342n54



Internal ID20136766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98142480..98143998hg38UCSC Ensembl
chr13:98794734..98796252hg19UCSC Ensembl
chr13:97592735..97594253hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381519
hg191519
hg181519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv562858, nsv562854, nsv562851, nsv562856, nsv562857, nsv562859, nsv562852, nsv562853
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3342n54
Frequency
Sample Size17421
Observed Gain16
Observed Loss0
Observed Complex0
Frequencyn/a


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