A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3557014



Internal ID18758090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33698858..33701106hg38UCSC Ensembl
Outerchr20:33698786..33701290hg38UCSC Ensembl
Innerchr20:32286664..32288912hg19UCSC Ensembl
Outerchr20:32286592..32289096hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382505
hg192505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9755761
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3557014
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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