A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275898



Internal ID20842938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100800818..100908581hg38UCSC Ensembl
chr8:101813046..101920809hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38107764
hg19107764
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567719
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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