A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3645446



Internal ID7032196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18838249..18932816hg38UCSC Ensembl
chr20:18818893..18913460hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3894568
hg1994568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv777e214
Supporting Variantsessv16154937
SamplesHG02513
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3645446
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