A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv189e214



Internal ID22756083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31681394..31740185hg38UCSC Ensembl
chr11:31702942..31761733hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3858792
hg1958792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3625836, esv3625838
SamplesHG00131
Known GenesELP4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv189e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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