A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645751



Internal ID7032499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37060566..37074965hg38UCSC Ensembl
chr20:35688969..35703368hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3814400
hg1914400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16179920, essv16179922, essv16179921
SamplesHG00277, HG01247, HG01097
Known GenesRBL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645751
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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