A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582429



Internal ID20955500
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 StatusM
Merged Variants
Supporting Variantsnssv18223087
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)nsv6582429
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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