A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645516



Internal ID7032265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23092851..23096634hg38UCSC Ensembl
Innerchr20:23092851..23096634hg38UCSC Ensembl
Outerchr20:23092607..23096909hg38UCSC Ensembl
chr20:23073488..23077271hg19UCSC Ensembl
Innerchr20:23073488..23077271hg19UCSC Ensembl
Outerchr20:23073244..23077546hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg383784
hg193784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16160682, essv16160681
SamplesNA19917, HG00657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645516
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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