A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567390



Internal ID20940461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121417657..121509459hg38UCSC Ensembl
chr8:122429897..122521699hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3891803
hg1991803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276070
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567390
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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