A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8452n54



Internal ID22776347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96247473..96321548hg38UCSC Ensembl
chr3:95966317..96040392hg19UCSC Ensembl
chr3:97449007..97523082hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3874076
hg1974076
hg1874076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv591036, nsv591035
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8452n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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