A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17382921



Internal ID22440791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21330941..21766277hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38435337
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971191
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17382921
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