A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106090



Internal ID22015323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140998211..141589189hg38UCSC Ensembl
chrX:140080376..140677316hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38590979
hg19596941
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639572
Samples
Known GenesLDOC1, SPANXA1, SPANXA2, SPANXA2-OT1, SPANXB1, SPANXB2, SPANXC, SPANXF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106090
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