A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14452884



Internal ID22254064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51669469..51713883hg38UCSC Ensembl
chrX:51412401..51456979hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3844415
hg1944579
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3243558
Supporting Variants
SamplesNA19238
Known GenesCENPVP1, CENPVP2
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14452884
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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