A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258299



Internal ID21399508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12027557..12275658hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38248102
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730234
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258299
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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