A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218462



Internal ID20785502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:8119377..8135412hg38UCSC Ensembl
chr11:8140924..8156959hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3816036
hg1916036
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576117
Supporting Variants
Samples
Known GenesRIC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218462
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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