A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100524



Internal ID22009757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:89773998..90077175hg38UCSC Ensembl
chr11:89507166..89810343hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38303178
hg19303178
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582427
Samples
Known GenesMIR5692A1, TRIM49, TRIM49C, TRIM49D1, TRIM49D2P, TRIM53AP, TRIM64, TRIM64B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100524
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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