A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18196224



Internal ID20763264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69815183..69824951hg38UCSC Ensembl
chr16:69849086..69858854hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389769
hg199769
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503918
Supporting Variants
Samples
Known GenesWWP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18196224
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00593


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