A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279059



Internal ID20846099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93720168..93720616hg38UCSC Ensembl
chr8:94732396..94732844hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571627
Supporting Variants
Samples
Known GenesFAM92A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279059
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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