A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616869



Internal ID7003755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34922437..34939113hg38UCSC Ensembl
chr8:34779955..34796631hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3816677
hg1916677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13165848
SamplesHG01973
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616869
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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