A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103890



Internal ID22013123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43467704..43467704hg38UCSC Ensembl
chr21:44887584..44887584hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647786
Samples
Known GenesLINC00313
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103890
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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