A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060372



Internal ID21969605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32845625..32845778hg38UCSC Ensembl
chr21:34217935..34218088hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060372
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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