A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5966690



Internal ID8944093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94168312..94177105hg38UCSC Ensembl
chr11:93901478..93910271hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg388794
hg198794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674143
Supporting Variants
SamplesNA19434
Known GenesPANX1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5966690
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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