A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275927



Internal ID20842967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102249358..102250214hg38UCSC Ensembl
chr8:103261586..103262442hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38857
hg19857
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275927
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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