A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5906505



Internal ID8883908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133287963..133291427hg38UCSC Ensembl
chr11:133157858..133161322hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383465
hg193465
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670789
Supporting Variants
SamplesNA19834
Known GenesOPCML
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5906505
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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