A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5576646



Internal ID9637273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20032015..20032459hg38UCSC Ensembl
chr20:20012659..20013103hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38445
hg19445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2665704
Supporting Variants
SamplesNA19372
Known GenesNAA20
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5576646
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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