A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5411269



Internal ID9123752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87385361..87387710hg38UCSC Ensembl
chr16:87418967..87421316hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382350
hg192350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658266
Supporting Variants
SamplesHG01137
Known GenesFBXO31
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5411269
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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