A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595866



Internal ID20968937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42837462..42837869hg38UCSC Ensembl
chr22:43233468..43233875hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4726n223
Supporting Variantsnssv18255039
Samples
Known GenesARFGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595866
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer