A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv773e199



Internal ID22758546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:378808..384510hg38UCSC Ensembl
chr20:359452..365154hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg385703
hg195703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2669966, esv2665049
SamplesNA18616
Known GenesTRIB3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv773e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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