A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659080



Internal ID9925185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19092118..19095002hg38UCSC Ensembl
Outerchr20:19091961..19095155hg38UCSC Ensembl
Innerchr20:19072762..19075646hg19UCSC Ensembl
Outerchr20:19072605..19075799hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg383195
hg193195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6192387, essv6035296, essv5771826
SamplesNA18633, HG00610, HG00463
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659080
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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