A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242759



Internal ID20809799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25287993..25288513hg38UCSC Ensembl
chr16:25299314..25299834hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242759
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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