A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240181



Internal ID20807221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81020818..81022048hg38UCSC Ensembl
chr16:81054423..81055653hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6583911
Supporting Variants
Samples
Known GenesCENPN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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