A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5429845



Internal ID208680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:362500..452351hg38UCSC Ensembl
chrX:323235..413086hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3889852
hg1989852
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735978
Samples
Known GenesPPP2R3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5429845
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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