A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616573



Internal ID7003459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20549443..20576924hg38UCSC Ensembl
chr8:20406954..20434435hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3827482
hg1927482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13132521
SamplesNA20774
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616573
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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