A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280437



Internal ID20489655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3477541..3477678hg38UCSC Ensembl
chr16:3527541..3527678hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743412
Supporting Variants
Samples
Known GenesNAA60
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280437
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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