A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17446167



Internal ID22504037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109139533..109140918hg38UCSC Ensembl
chr9:111901813..111903198hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381386
hg191386
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973484
Supporting Variants
Samples
Known GenesFRRS1L
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17446167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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