A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13998734



Internal ID3537600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4366254..4516593hg38UCSC Ensembl
chr11:4387484..4537823hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38150340
hg19150340
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625179
Supporting Variants
SamplesHG03126
Known GenesOR52B4, OR52K1, OR52K2, TRIM21
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13998734
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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