A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058620



Internal ID21967853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31281434..31380362hg38UCSC Ensembl
chr21:32653749..32752676hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3898929
hg1998928
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640848
Samples
Known GenesTIAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058620
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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