A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616688



Internal ID7003574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25654477..25738502hg38UCSC Ensembl
chr8:25511993..25596018hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3884026
hg1984026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13147678, essv13147677, essv13147676
SamplesHG01242, HG01164, HG02345
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616688
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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