A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050981



Internal ID21960215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45155565..45156377hg38UCSC Ensembl
chr21:46575480..46576292hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649804
Samples
Known GenesADARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050981
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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