A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5640098



Internal ID9885451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:385360..399238hg38UCSC Ensembl
chr20:366004..379882hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3813879
hg1913879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657243
Supporting Variants
SamplesNA20760
Known GenesTRIB3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5640098
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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