A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667972



Internal ID21616279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45918429..45918429hg38UCSC Ensembl
chr20:44547068..44547068hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116684
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667972
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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