A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1008032



Internal ID7073126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63792827..63802371hg38UCSC Ensembl
Outerchr20:62424180..62433724hg19UCSC Ensembl
Outerchr20:61894624..61904168hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg389545
hg199545
hg189545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565729
SamplesHuRef
Known GenesZBTB46
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1008032
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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