A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626978



Internal ID7013808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82020945..82057572hg38UCSC Ensembl
chr11:81731987..81768614hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3836628
hg1936628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14218104
SamplesNA12763
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626978
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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