A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv280n21



Internal ID22766472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35965622..35977275hg38UCSC Ensembl
chr3:36007114..36018767hg19UCSC Ensembl
chr3:35982118..35993771hg18UCSC Ensembl
chr3:35982118..35993771hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3811654
hg1911654
hg1811654
hg1711654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv519232, nsv526585
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv280n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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