A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432633



Internal ID211371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:117674690..117674797hg38UCSC Ensembl
chrX:116808653..116808760hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432633
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