A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267883



Internal ID20477101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45007803..45007803hg38UCSC Ensembl
chr21:46427718..46427718hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267883
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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