A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427932



Internal ID206816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90413527..90414047hg38UCSC Ensembl
chrX:89668526..89669046hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427932
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