A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16160041



Internal ID2805177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22344810..22349612hg38UCSC Ensembl
Innerchr20:22344819..22349603hg38UCSC Ensembl
Outerchr20:22344801..22349621hg38UCSC Ensembl
chr20:22325448..22330250hg19UCSC Ensembl
Innerchr20:22325457..22330241hg19UCSC Ensembl
Outerchr20:22325439..22330259hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384803
hg194803
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645503
Supporting Variants
SamplesHG02477
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16160041
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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