A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645887



Internal ID7032635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43658261..43666033hg38UCSC Ensembl
Innerchr20:43658761..43665533hg38UCSC Ensembl
Outerchr20:43657261..43667033hg38UCSC Ensembl
chr20:42286901..42294673hg19UCSC Ensembl
Innerchr20:42287401..42294173hg19UCSC Ensembl
Outerchr20:42285901..42295673hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg387773
hg197773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16192719
SamplesHG01967
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645887
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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