A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599138



Internal ID20972209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11374031..11376868hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382838
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4613n223
Supporting Variantsnssv18254269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599138
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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