A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5617959



Internal ID21566264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33329513..33329513hg38UCSC Ensembl
chr3:33371005..33371005hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17121960
SamplesHG00171
Known GenesFBXL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5617959
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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