A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426592



Internal ID205521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:41203947..41204018hg38UCSC Ensembl
chrX:41063200..41063271hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17736551
Samples
Known GenesUSP9X
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426592
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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