A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16160680



Internal ID6162496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:23058998..23075316hg38UCSC Ensembl
Innerchr20:23058998..23075316hg38UCSC Ensembl
Outerchr20:23058498..23075816hg38UCSC Ensembl
chr20:23039635..23055953hg19UCSC Ensembl
Innerchr20:23039635..23055953hg19UCSC Ensembl
Outerchr20:23039135..23056453hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3816319
hg1916319
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645515
Supporting Variants
SamplesHG03645
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16160680
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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