A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608184



Internal ID21556489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33344519..33344519hg38UCSC Ensembl
chr3:33386011..33386011hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124740
SamplesHG00171
Known GenesFBXL2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608184
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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