A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2855236



Internal ID10528216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:63218616..63218828hg38UCSC Ensembl
Outerchr18:60885849..60886061hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7124803
SamplesHuRef
Known GenesBCL2
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv2855236
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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