A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740886



Internal ID20516863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60047206..60064656hg38UCSC Ensembl
chr16:60081110..60098560hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3817451
hg1917451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285323
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740886
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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