A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223087



Internal ID20790127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93899951..96855215hg38UCSC Ensembl
chr11:93633117..96726215hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382955265
hg193093099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582429
Supporting Variants
Samples
Known GenesAMOTL1, ANKRD49, CCDC82, CEP57, CWC15, ENDOD1, FAM76B, FOLR4, FUT4, GPR83, HEPHL1, JRKL, JRKL-AS1, KDM4D, KDM4E, LOC643037, MAML2, MIR1260B, MRE11A, MTMR2, PANX1, PIWIL4, SESN3, SRSF8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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