A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625193



Internal ID7012028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4786330..4890472hg38UCSC Ensembl
chr11:4807560..4911702hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38104143
hg19104143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13999295, essv13999294
SamplesNA20521, NA20807
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625193
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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