A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645890



Internal ID6685951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43688953..43690813hg38UCSC Ensembl
Innerchr20:43689000..43690766hg38UCSC Ensembl
Outerchr20:43688906..43690860hg38UCSC Ensembl
chr20:42317593..42319453hg19UCSC Ensembl
Innerchr20:42317640..42319406hg19UCSC Ensembl
Outerchr20:42317546..42319500hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381861
hg191861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16192787
SamplesNA18945
Known GenesMYBL2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645890
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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