A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6567093



Internal ID20940164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94377777..94437353hg38UCSC Ensembl
chr8:95390005..95449581hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3859577
hg1959577
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279083
Samples
Known GenesFSBP, RAD54B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6567093
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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