A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5918092



Internal ID8895495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94177637..94178077hg38UCSC Ensembl
chr11:93910803..93911243hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656589
Supporting Variants
SamplesHG00263
Known GenesPANX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5918092
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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