A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625179



Internal ID7012014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4366254..4516593hg38UCSC Ensembl
chr11:4387484..4537823hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38150340
hg19150340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13998735, essv13998734
SamplesHG03126, HG03132
Known GenesOR52B4, OR52K1, OR52K2, TRIM21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625179
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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