A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453237



Internal ID22129172
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
SamplesHG00512
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B
MethodSequencing
AnalysisSingle strand sequencing, and assortment analysis
PlatformStrand-seq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453237
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