A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663618



Internal ID21611923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55331803..55331803hg38UCSC Ensembl
chr14:55798521..55798521hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38630
hg19630
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081268, nssv17097085, nssv17090130
SamplesHG03486, NA19238, HG00731
Known GenesFBXO34
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663618
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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