A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18240059



Internal ID20807099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63650454..63651180hg38UCSC Ensembl
chr16:63684358..63685084hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593122
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18240059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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