A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16175888



Internal ID2881762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33964446..33966614hg38UCSC Ensembl
Innerchr20:33964483..33966578hg38UCSC Ensembl
Outerchr20:33964410..33966651hg38UCSC Ensembl
chr20:32552252..32554420hg19UCSC Ensembl
Innerchr20:32552289..32554384hg19UCSC Ensembl
Outerchr20:32552216..32554457hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382169
hg192169
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645692
Supporting Variants
SamplesHG02557
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16175888
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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