A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16160681



Internal ID1039819
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645516
Supporting Variants
SamplesHG00657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16160681
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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