A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663066



Internal ID21611371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:86243705..86243705hg38UCSC Ensembl
chr14:86710049..86710049hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081961
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663066
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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