A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12428n54



Internal ID20145852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143616727..143626978hg38UCSC Ensembl
chr8:144698897..144709148hg19UCSC Ensembl
chr8:144770040..144780291hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3810252
hg1910252
hg1810252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv612863, nsv612870, nsv612853, nsv612858, nsv612859
Samples
Known GenesTSTA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12428n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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