A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645918



Internal ID7032666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44849207..44855808hg38UCSC Ensembl
Innerchr20:44849256..44855759hg38UCSC Ensembl
Outerchr20:44849158..44855857hg38UCSC Ensembl
chr20:43477848..43484449hg19UCSC Ensembl
Innerchr20:43477897..43484400hg19UCSC Ensembl
Outerchr20:43477799..43484498hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386602
hg196602
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16195995
SamplesHG00446
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645918
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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