A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106987



Internal ID22016221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41672809..41672809hg38UCSC Ensembl
chr21:43092969..43092969hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381053
hg191053
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639097
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106987
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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