A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646593



Internal ID21594898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74828748..74828748hg38UCSC Ensembl
chr18:72540704..72540704hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17101984
SamplesHG03732
Known GenesZNF407
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646593
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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