A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599961



Internal ID20973032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:40269154..40269872hg38UCSC Ensembl
chr22:40665158..40665876hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38719
hg19719
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253787
Samples
Known GenesTNRC6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599961
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