A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14317696



Internal ID4319515
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3628131
Supporting Variants
SamplesNA21133
Known GenesOPCML
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14317696
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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