A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646234



Internal ID7032979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59852288..59859678hg38UCSC Ensembl
Innerchr20:59852288..59859678hg38UCSC Ensembl
Outerchr20:59852191..59859771hg38UCSC Ensembl
chr20:58427343..58434733hg19UCSC Ensembl
Innerchr20:58427343..58434733hg19UCSC Ensembl
Outerchr20:58427246..58434826hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg387391
hg197391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16219071
SamplesHG01858
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646234
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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