A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244333



Internal ID20811373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69343931..69344869hg38UCSC Ensembl
chr16:69377834..69378772hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38939
hg19939
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6587581
Supporting Variants
Samples
Known GenesTMED6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244333
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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