A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422105



Internal ID201158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9805511..9808609hg38UCSC Ensembl
chrX:9773551..9776649hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg383099
hg193099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739205
Samples
Known GenesSHROOM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422105
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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