A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667295



Internal ID21615602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:45866822..45866822hg38UCSC Ensembl
chr20:44495461..44495461hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116681
SamplesHG02818
Known GenesZSWIM3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667295
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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