A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645883



Internal ID7032631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43441859..43448600hg38UCSC Ensembl
Innerchr20:43441878..43448581hg38UCSC Ensembl
Outerchr20:43441840..43448619hg38UCSC Ensembl
chr20:42070499..42077240hg19UCSC Ensembl
Innerchr20:42070518..42077221hg19UCSC Ensembl
Outerchr20:42070480..42077259hg19UCSC Ensembl
Cytoband20q13.11
Allele length
AssemblyAllele length
hg386742
hg196742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16190330, essv16190329
SamplesHG01405, HG03303
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645883
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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