A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738016



Internal ID20513982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49954426..49954693hg38UCSC Ensembl
chr16:49988337..49988604hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738016
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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