A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275553



Internal ID20484771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52248857..52248857hg38UCSC Ensembl
chr16:52282769..52282769hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765750
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275553
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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