A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3069346



Internal ID11089012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:32739619..32740291hg38UCSC Ensembl
Outerchr20:31327426..31328098hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7338913
SamplesHuRef
Known GenesCOMMD7
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3069346
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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