A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv100e201



Internal ID6312611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6252575..6252957hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsesv2731940, esv2743008
SamplesSSM043, SSM072, SSM020, SSM017, SSM028, SSM021, SSM063, SSM018
Known GenesPFKFB3
Method
Analysis
Platform
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)dgv100e201
Frequency
Sample Size96
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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