A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112624



Internal ID22021857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45224516..45224516hg38UCSC Ensembl
chr21:46644431..46644431hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638458
Samples
Known GenesADARB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112624
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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