A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278864



Internal ID20845904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8301482..8322264hg38UCSC Ensembl
chr8:8159004..8179780hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3820783
hg1920777
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6570514
Supporting Variants
Samples
Known GenesSGK223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278864
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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