A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625226



Internal ID6665374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5414714..5440279hg38UCSC Ensembl
Innerchr11:5414714..5440279hg38UCSC Ensembl
Outerchr11:5414214..5440779hg38UCSC Ensembl
chr11:5435944..5461509hg19UCSC Ensembl
Innerchr11:5435944..5461509hg19UCSC Ensembl
Outerchr11:5435444..5462009hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3825566
hg1925566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14003366, essv14003365
SamplesNA19066, NA18966
Known GenesOR51B5, OR51Q1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625226
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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