A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14003373



Internal ID4005189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5464023..5571817hg38UCSC Ensembl
chr11:5485253..5593047hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38107795
hg19107795
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625230
Supporting Variants
SamplesHG01851
Known GenesOR51B5, OR52D1, OR52H1, UBQLN3, UBQLNL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14003373
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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