A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181899



Internal ID20748939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12219201..12228700hg38UCSC Ensembl
chr18:12219200..12228699hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528998
Supporting Variants
Samples
Known GenesC18orf61
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181899
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00079


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