A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281278



Internal ID20490496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9027178..9027178hg38UCSC Ensembl
chr21:9866011..9866011hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281278
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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