A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5669405



Internal ID21617711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63808066..63808066hg38UCSC Ensembl
chr20:62439419..62439419hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117769
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5669405
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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