A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12016n54



Internal ID20145440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:15544498..15552706hg38UCSC Ensembl
chr8:15402007..15410215hg19UCSC Ensembl
chr8:15446378..15454586hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388209
hg198209
hg188209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610537, nsv610543
Samples
Known GenesTUSC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12016n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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