A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1910e59



Internal ID18987411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63197939..63200537hg38UCSC Ensembl
chr18:60865172..60867770hg19UCSC Ensembl
chr18:59016152..59018750hg18UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg382599
hg192599
hg182599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3337809, esv3435745
SamplesNA19239, NA19240
Known GenesBCL2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1910e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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