A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8364n54



Internal ID22776259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66864334..66889990hg38UCSC Ensembl
chr3:66914758..66940414hg19UCSC Ensembl
chr3:66997448..67023104hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3825657
hg1925657
hg1825657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590559, nsv590558
SamplesHGDP01163
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8364n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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