A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355332



Internal ID22581001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66252469..66253352hg38UCSC Ensembl
chr11:66019940..66020823hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38884
hg19884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973850
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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