A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239290



Internal ID20806331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55764978..55828704hg38UCSC Ensembl
chr16:55798890..55862616hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3863727
hg1963727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587849
Supporting Variants
Samples
Known GenesCES1, CES1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239290
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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