A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426741



Internal ID205663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151972537..151972928hg38UCSC Ensembl
chrX:151141009..151141400hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738000
Samples
Known GenesGABRE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426741
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