A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561875



Internal ID334842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107778058..107778074hg38UCSC Ensembl
chrX:107021288..107021304hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3817
hg1917
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741878
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561875
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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