A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14105333



Internal ID4077475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41089649..41149604hg38UCSC Ensembl
chr11:41111199..41171154hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3859956
hg1959956
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3626081
Supporting Variants
SamplesHG03708
Known GenesLRRC4C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14105333
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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