A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594775



Internal ID20967846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69431105..69431545hg38UCSC Ensembl
chr16:69465008..69465448hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38441
hg19441
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244341
Samples
Known GenesCYB5B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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