A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706420



Internal ID130086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4109859..4124106hg38UCSC Ensembl
chr16:4159860..4174107hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3814248
hg1914248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528946
Supporting Variants
Samples
Known GenesADCY9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706420
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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