A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239990



Internal ID20807030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3555416..3555718hg38UCSC Ensembl
chr16:3605417..3605719hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586639
Supporting Variants
Samples
Known GenesNLRC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239990
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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