A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18276991



Internal ID20844031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114422129..114426951hg38UCSC Ensembl
chr8:115434358..115439180hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg384823
hg194823
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18276991
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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