A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8142n54



Internal ID20141566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21733..143598hg38UCSC Ensembl
chr3:63411..185281hg19UCSC Ensembl
chr3:38411..160281hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38121866
hg19121871
hg18121871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv589236, nsv589241, nsv589234
SamplesHGDP00183, HGDP00096, HGDP00208
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8142n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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