A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645568



Internal ID7032317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24884958..24920564hg38UCSC Ensembl
chr20:24865594..24901200hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3835607
hg1935607
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16164053, essv16164054
SamplesHG03539, HG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645568
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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