A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16265059



Internal ID20474277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62983803..62984053hg38UCSC Ensembl
chr16:63017707..63017957hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733263
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16265059
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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