A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3627679



Internal ID6667826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108509006..108580807hg38UCSC Ensembl
chr11:108379733..108451534hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3871802
hg1971802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14278416
SamplesHG00692
Known GenesEXPH5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3627679
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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