A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12441n54



Internal ID20145865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144492696..144495299hg38UCSC Ensembl
chr8:145718079..145720682hg19UCSC Ensembl
chr8:145688887..145691490hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg382604
hg192604
hg182604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv612952, nsv612954
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12441n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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