A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054661



Internal ID21963895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38913722..38914408hg38UCSC Ensembl
chr21:40285646..40286332hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647327
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054661
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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