A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv294n21



Internal ID22766486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101587663..101595096hg38UCSC Ensembl
chr3:101306507..101313940hg19UCSC Ensembl
chr3:102789197..102796630hg18UCSC Ensembl
chr3:102789197..102796630hg17UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg387434
hg197434
hg187434
hg177434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv528547, nsv522745
Samples
Known GenesPCNP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv294n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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