A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663063



Internal ID21611368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:54903940..54903940hg38UCSC Ensembl
chr14:55370658..55370658hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098156
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663063
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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