A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392815



Internal ID22450685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:49632857..49656407hg38UCSC Ensembl
chr22:50026505..50050055hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3823551
hg1923551
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5972113
Supporting Variants
Samples
Known GenesC22orf34
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392815
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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