A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646563



Internal ID21594868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:55456367..55456367hg38UCSC Ensembl
chr14:55923085..55923085hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094710
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646563
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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