A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426825



Internal ID205741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:57985930..57986882hg38UCSC Ensembl
chrX:58012364..58013316hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38953
hg19953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426825
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