A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594027



Internal ID20967098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67565237..67565472hg38UCSC Ensembl
chr16:67599140..67599375hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38236
hg19236
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243615
Samples
Known GenesCTCF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594027
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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