A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18277096



Internal ID20844136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:119884658..119886670hg38UCSC Ensembl
chr8:120896898..120898910hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg382013
hg192013
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570413
Supporting Variants
Samples
Known GenesDEPTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18277096
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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