A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5961098



Internal ID22736058
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 Variantsnssv17410832
Samples
Known GenesFBXL2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5961098
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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