A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5759001



Internal ID8736404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132696439..132705393hg38UCSC Ensembl
chr11:132566334..132575288hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg388955
hg198955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657031
Supporting Variants
SamplesHG01204
Known GenesOPCML
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5759001
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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