A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520307



Internal ID296637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71546000..71556682hg38UCSC Ensembl
chr16:71579903..71590585hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3810683
hg1910683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17708578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520307
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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