A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6559312



Internal ID20932383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100143799..100146616hg38UCSC Ensembl
chr8:101156027..101158844hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg382818
hg192818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275877
Samples
Known GenesFBXO43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6559312
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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