A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227863



Internal ID20794903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65284774..65285254hg38UCSC Ensembl
chr11:65052245..65052725hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38481
hg19481
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588039
Supporting Variants
Samples
Known GenesPOLA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227863
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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