A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17709134



Internal ID132800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75669958..75674828hg38UCSC Ensembl
chr16:75703856..75708726hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg384871
hg194871
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5523407
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17709134
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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