A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14165659



Internal ID3576002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:55985222..56112918hg38UCSC Ensembl
chr11:55752698..55880394hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38127697
hg19127697
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626466
Supporting Variants
SamplesHG03163
Known GenesOR5AS1, OR5F1, OR7E5P, OR8H2, OR8I2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14165659
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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