A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615785



Internal ID7002673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:379703..434511hg38UCSC Ensembl
chr8:329703..384511hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3854809
hg1954809
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13054203, essv13054202, essv13054204, essv13054201
SamplesHG02536, NA19209, HG02010, NA20520
Known GenesFAM87A, FBXO25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615785
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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