A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645558



Internal ID7032307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24707523..24715595hg38UCSC Ensembl
Innerchr20:24707526..24715592hg38UCSC Ensembl
Outerchr20:24707520..24715598hg38UCSC Ensembl
chr20:24688159..24696231hg19UCSC Ensembl
Innerchr20:24688162..24696228hg19UCSC Ensembl
Outerchr20:24688156..24696234hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg388073
hg198073
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16163975
SamplesHG01799
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645558
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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