A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17388043



Internal ID22445913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69815183..69824950hg38UCSC Ensembl
chr16:69849086..69858853hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg389768
hg199768
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5932440
Supporting Variants
Samples
Known GenesWWP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17388043
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003


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