A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051803



Internal ID21961036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9811650..9839846hg38UCSC Ensembl
chr4_gl000193_random:78964..107160hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3828197
hg1928197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051803
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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