A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12361n54



Internal ID22780256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139740045..139750704hg38UCSC Ensembl
chr8:140752288..140762947hg19UCSC Ensembl
chr8:140821470..140832129hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3810660
hg1910660
hg1810660
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv612547, nsv612546
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12361n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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