A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14161555



Internal ID4163371
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626446
Supporting Variants
SamplesHG03563
Known GenesOR4C11, OR4P4, OR4S2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14161555
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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