A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279040



Internal ID20846080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92150859..92151957hg38UCSC Ensembl
chr8:93163087..93164185hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381099
hg191099
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279040
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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