A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626446



Internal ID6666595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55600896..55659493hg38UCSC Ensembl
chr11:55368372..55426969hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3858598
hg1958598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14161555, essv14161554
SamplesHG03563, HG01624
Known GenesOR4C11, OR4P4, OR4S2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626446
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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