A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422754



Internal ID201790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154647606..154653606hg38UCSC Ensembl
chrX:153875880..153881880hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738142
Samples
Known GenesCTAG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422754
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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