A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14464201



Internal ID22253656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135147415..135225242hg38UCSC Ensembl
chrX:134281342..134359186hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3877828
hg1977845
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3546569
Supporting Variants
SamplesNA19238
Known GenesCXorf48
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14464201
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