A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240660



Internal ID20807700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4759637..4763320hg38UCSC Ensembl
chr16:4809638..4813321hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594330
Supporting Variants
Samples
Known GenesZNF500
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240660
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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