A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976035



Internal ID22750970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:116678656..116911087hg38UCSC Ensembl
chrX:115812624..116045055hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38232432
hg19232432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17448512
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT2]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976035
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