A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665383



Internal ID9931488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108469066..108470770hg38UCSC Ensembl
chr11:108339793..108341497hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5584188, essv6004052, essv5485307, essv5576080
SamplesNA19377, NA19379, NA19401, NA19473
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665383
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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