A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12013n54



Internal ID22779908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15531057..15554099hg38UCSC Ensembl
chr8:15388566..15411608hg19UCSC Ensembl
chr8:15432937..15455979hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3823043
hg1923043
hg1823043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610530, nsv610531
SamplesHGDP00274
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12013n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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