A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5424697



Internal ID203676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:23772333..23776016hg38UCSC Ensembl
chrX:23790450..23794133hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5424697
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer