A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18243592



Internal ID20810632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67045516..67045826hg38UCSC Ensembl
chr16:67079419..67079729hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578720
Supporting Variants
Samples
Known GenesCBFB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18243592
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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