A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551217



Internal ID324694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169961638..169961676hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3875
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991090
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551217
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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