A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666055



Internal ID21614360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:61793794..61793794hg38UCSC Ensembl
chr20:60368850..60368850hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117401
SamplesHG00513
Known GenesCDH4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666055
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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