A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258323



Internal ID21400363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149578223..149597276hg38UCSC Ensembl
chrX:148659879..148678936hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3819054
hg1919058
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesNA19239
Known GenesHSFX1, HSFX2, MAGEA9, MAGEA9B, TMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258323
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