A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567518



Internal ID20940589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80561407..80562533hg38UCSC Ensembl
chr8:81473642..81474768hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278817
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567518
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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