A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4738774



Internal ID20514745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69325384..69325454hg38UCSC Ensembl
chr16:69359287..69359357hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290013
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4738774
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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