A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2422304



Internal ID7906401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:14719164..14945651hg38UCSC Ensembl
Innerchr20:14699810..14926297hg19UCSC Ensembl
Innerchr20:14647810..14874297hg18UCSC Ensembl
Innerchr20:14647810..14874297hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38226488
hg19226488
hg18226488
hg17226488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5161288
SamplesND03938
Known GenesMACROD2, MACROD2-AS1
MethodSNP array
Analysislog R ratio and B allele frequency.
PlatformNot specified
Comments
ReferenceSimon-Sanchez_et_al_2007
Pubmed ID17116639
Accession Number(s)esv2422304
Frequency
Sample Size181
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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