A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592068



Internal ID20965139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69159331..69159461hg38UCSC Ensembl
chr16:69193234..69193364hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244313
Samples
Known GenesCIRH1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592068
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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