A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17706389



Internal ID130055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3706572..3707249hg38UCSC Ensembl
chr16:3756573..3757250hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38678
hg19678
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529479
Supporting Variants
Samples
Known GenesTRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17706389
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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