A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14464046



Internal ID22262588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154581225..154633196hg38UCSC Ensembl
chrX:153809488..153861459hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3851972
hg1951972
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3246958
Supporting Variants
SamplesNA19238
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14464046
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