A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427233



Internal ID206140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:65685501..65702389hg38UCSC Ensembl
chrX:64905362..64922251hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3816889
hg1916890
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740406
Samples
Known GenesMSN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427233
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