A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666193



Internal ID21614498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18246600..18268271hg38UCSC Ensembl
chr11:18268147..18289818hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821672
hg1921672
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073841
Samples
Known GenesSAA1, SAA2, SAA2-SAA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666193
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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