A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222671



Internal ID20789711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25281982..25498896hg38UCSC Ensembl
chr11:25303528..25520442hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38216915
hg19216915
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578759
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222671
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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