A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275882



Internal ID20842922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100188410..100189246hg38UCSC Ensembl
chr8:101200638..101201474hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563304
Supporting Variants
Samples
Known GenesSPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275882
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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