A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623955



Internal ID7010811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80722354..80742745hg38UCSC Ensembl
chr10:82482110..82502501hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3820392
hg1920392
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13870832, essv13870831
SamplesHG01456, HG01139
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623955
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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