A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257995



Internal ID21399048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18796714..18823108hg38UCSC Ensembl
chr22:18784227..18810621hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3826395
hg1926395
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730176
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257995
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