A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18278147



Internal ID20845187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:49814099..49821533hg38UCSC Ensembl
chr8:50726659..50734093hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg387435
hg197435
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18278147
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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