A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13999295



Internal ID6663621
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625193
Supporting Variants
SamplesNA20807
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13999295
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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