A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217160



Internal ID20784200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61650332..61652807hg38UCSC Ensembl
chr11:61417804..61420279hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382476
hg192476
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217160
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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