A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041222



Internal ID21950558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45133747..45134361hg38UCSC Ensembl
chr21:46553662..46554276hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38615
hg19615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648440
Samples
Known GenesADARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041222
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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