A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12018n54



Internal ID20145442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15546943..15554587hg38UCSC Ensembl
chr8:15404452..15412096hg19UCSC Ensembl
chr8:15448823..15456467hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg387645
hg197645
hg187645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610553, nsv610551, nsv610552, nsv610550
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12018n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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