A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105030



Internal ID22014264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46228839..46228839hg38UCSC Ensembl
chr21:47648753..47648753hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105030
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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