A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272822



Internal ID20839862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99372202..99372739hg38UCSC Ensembl
chr6:99820078..99820615hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572525
Supporting Variants
Samples
Known GenesCOQ3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272822
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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