A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426595



Internal ID205524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:5533878..5559601hg38UCSC Ensembl
chrX:5451919..5477642hg19UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3825724
hg1925724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426595
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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