A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374905



Internal ID22600574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98535023..98562713hg38UCSC Ensembl
chr13:99187277..99214967hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3827691
hg1927691
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971737
Supporting Variants
Samples
Known GenesSTK24
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374905
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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