A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278086



Internal ID20845126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:43036620..43037453hg38UCSC Ensembl
chr8:42891763..42892596hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38834
hg19834
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278086
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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