A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17641432



Internal ID21833479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45584585..45584585hg38UCSC Ensembl
chr21:47004499..47004499hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109031
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17641432
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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