A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv21e209



Internal ID22760882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52991984..53004882hg38UCSC Ensembl
chr3:53026000..53038898hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3812899
hg1912899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3197123, esv2836680
SamplesHuRef
Known GenesSFMBT1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)dgv21e209
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer