A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6563289



Internal ID20936360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77973274..77973888hg38UCSC Ensembl
chr8:78885509..78886123hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18278756
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6563289
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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