A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17437051



Internal ID22494921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118986508..118989217hg38UCSC Ensembl
chr9:121748786..121751495hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg382710
hg192710
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973248
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17437051
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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