A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14003368



Internal ID4005184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5446102..5467479hg38UCSC Ensembl
Innerchr11:5446102..5467479hg38UCSC Ensembl
Outerchr11:5445602..5467979hg38UCSC Ensembl
chr11:5467332..5488709hg19UCSC Ensembl
Innerchr11:5467332..5488709hg19UCSC Ensembl
Outerchr11:5466832..5489209hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3821378
hg1921378
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625227
Supporting Variants
SamplesNA19066
Known GenesOR51B5, OR51I2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14003368
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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