A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599771



Internal ID20972842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36105612..36614161hg38UCSC Ensembl
chr22:36501660..37010208hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38508550
hg19508549
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18255212
Samples
Known GenesAPOL1, APOL2, APOL3, APOL4, CACNG2, EIF3D, FOXRED2, MIR6819, MYH9, TXN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599771
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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