A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109773



Internal ID22019006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:131679246..131842280hg38UCSC Ensembl
chrX:130813260..130976308hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg38163035
hg19163049
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638209
Samples
Known GenesLOC286467
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109773
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