A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230398



Internal ID20797438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89806033..90084028hg38UCSC Ensembl
chr11:89539201..89817196hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38277996
hg19277996
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591612
Supporting Variants
Samples
Known GenesMIR5692A1, TRIM49, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230398
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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