A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14003363



Internal ID4005179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5408083..5472058hg38UCSC Ensembl
chr11:5429313..5493288hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3863976
hg1963976
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625225
Supporting Variants
SamplesNA18966
Known GenesOR51B5, OR51I1, OR51I2, OR51Q1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14003363
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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