A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10904n54



Internal ID22778799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108559308..108561930hg38UCSC Ensembl
chr6:108880511..108883133hg19UCSC Ensembl
chr6:108987204..108989826hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382623
hg192623
hg182623
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv604478, nsv604480, nsv604481, nsv604479
Samples
Known GenesFOXO3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10904n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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