A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669966



Internal ID9936071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:378808..384466hg38UCSC Ensembl
chr20:359452..365110hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385659
hg195659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv773e199
Supporting Variantsessv6547778
SamplesNA18616
Known GenesTRIB3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669966
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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