A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280832



Internal ID20490050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74828745..74828745hg38UCSC Ensembl
chr18:72540701..72540701hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756158
Supporting Variants
Samples
Known GenesZNF407
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280832
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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