A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281403



Internal ID20848443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91412636..91413368hg38UCSC Ensembl
chr9:94174918..94175650hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560216
Supporting Variants
Samples
Known GenesNFIL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281403
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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