A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166832



Internal ID21492687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:356822..356822hg38UCSC Ensembl
chrX:317557..317557hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616194
Supporting Variants
SamplesNA19238
Known GenesPPP2R3B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166832
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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