A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422492



Internal ID201535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:106219976..106520935hg38UCSC Ensembl
chrX:105463969..105764165hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38300960
hg19300197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741819
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422492
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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