A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17643572



Internal ID21835619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152809451..153071349hg38UCSC Ensembl
chrX:151977983..152239732hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38261899
hg19261750
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106247
Supporting Variants
Samples
Known GenesCETN2, NSDHL, PNMA3, PNMA5, ZNF185
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17643572
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer