A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5978876



Internal ID22753811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47517952..47521795hg38UCSC Ensembl
chrX:47377351..47381194hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg383844
hg193844
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461686
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5978876
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