A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557108



Internal ID18758184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:44047494..44047881hg38UCSC Ensembl
Outerchr20:44047401..44047933hg38UCSC Ensembl
Innerchr20:42676134..42676521hg19UCSC Ensembl
Outerchr20:42676041..42676573hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755855
Samples
Known GenesTOX2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557108
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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