A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645478



Internal ID7032228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20306601..20346658hg38UCSC Ensembl
chr20:20287245..20327302hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3840058
hg1940058
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16155650
SamplesHG01605
Known GenesC20orf26
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645478
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer