A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16166529



Internal ID6025527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25703073..25713676hg38UCSC Ensembl
chr20:25683709..25694312hg19UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3810604
hg1910604
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3645593
Supporting Variants
SamplesNA19435
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16166529
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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