A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3628131



Internal ID6668275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132800717..132811364hg38UCSC Ensembl
Innerchr11:132801217..132810864hg38UCSC Ensembl
Outerchr11:132799717..132812364hg38UCSC Ensembl
chr11:132670612..132681259hg19UCSC Ensembl
Innerchr11:132671112..132680759hg19UCSC Ensembl
Outerchr11:132669612..132682259hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3810648
hg1910648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14317696
SamplesNA21133
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3628131
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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