A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615786



Internal ID7002674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:424430..464668hg38UCSC Ensembl
chr8:374430..414668hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3840239
hg1940239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13054208, essv13054206, essv13054205, essv13054207
SamplesHG02536, NA19209, HG02010, NA20520
Known GenesFBXO25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615786
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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