A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258406



Internal ID21399560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76146142..76148988hg38UCSC Ensembl
chrX:75365977..75368823hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg382847
hg192847
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730272
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258406
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