A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14460792



Internal ID22129814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89744798..90095507hg38UCSC Ensembl
chr11:89477966..89828675hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38350710
hg19350710
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3246394
Supporting Variants
SamplesHG00513
Known GenesMIR5692A1, TRIM49, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B, UBTFL1
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14460792
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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