A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17708456



Internal ID132122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87270753..87285988hg38UCSC Ensembl
chr16:87304359..87319594hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3815236
hg1915236
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5529243
Supporting Variants
Samples
Known GenesLOC101928682
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17708456
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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