A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530919



Internal ID306887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20106076..20106863hg38UCSC Ensembl
chr16:20117398..20118185hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38788
hg19788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17706163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530919
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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