A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422774



Internal ID201809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85635139..85641947hg38UCSC Ensembl
chrX:84890144..84896952hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg386809
hg196809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422774
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