A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980112



Internal ID22755047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:84840993..84890016hg38UCSC Ensembl
chrX:84096000..84145022hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg3849024
hg1949023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468933
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980112
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