A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5525898



Internal ID302045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67315407..67315740hg38UCSC Ensembl
chr16:67349310..67349643hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707493
Samples
Known GenesKCTD19
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5525898
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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