A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281547



Internal ID20848587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96360346..96360996hg38UCSC Ensembl
chr9:99122628..99123278hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562834
Supporting Variants
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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