A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105156



Internal ID22014390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46699306..46699306hg38UCSC Ensembl
chr21:48119218..48119218hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105156
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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