A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258063



Internal ID21399071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55457117..55516109hg38UCSC Ensembl
chrX:55483550..55542542hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3858993
hg1958993
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730209
Supporting Variants
SamplesHG00731
Known GenesUSP51
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258063
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