A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616630



Internal ID6656826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23162890..23197198hg38UCSC Ensembl
chr8:23020403..23054711hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3834309
hg1934309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13134735
SamplesHG02371
Known GenesTNFRSF10A, TNFRSF10D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616630
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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