A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280109



Internal ID20847149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132902384..132906971hg38UCSC Ensembl
chr9:135777771..135782358hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg384588
hg194588
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575186
Supporting Variants
Samples
Known GenesTSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280109
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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