A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6026333



Internal ID8911223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1033167..1036693hg38UCSC Ensembl
Outerchr20:1033130..1036743hg38UCSC Ensembl
Innerchr20:1013810..1017336hg19UCSC Ensembl
Outerchr20:1013773..1017386hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg383614
hg193614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666390
Supporting Variants
SamplesHG00375
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6026333
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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