A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17710282



Internal ID133948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85484380..85541354hg38UCSC Ensembl
chr16:85517986..85574960hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3856975
hg1956975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5525772
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17710282
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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