A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668088



Internal ID21616394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35928297..35928297hg38UCSC Ensembl
chr20:34516219..34516219hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116871
SamplesHG03732
Known GenesPHF20
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668088
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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