A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv272n21



Internal ID20131993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4080585..4319799hg38UCSC Ensembl
chr3:4122269..4361483hg19UCSC Ensembl
chr3:4097269..4336483hg18UCSC Ensembl
chr3:4097269..4336483hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38239215
hg19239215
hg18239215
hg17239215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv522239, nsv516589
Samples
Known GenesSETMAR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv272n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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