A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560729



Internal ID333728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22669739..22669789hg38UCSC Ensembl
chr6:22669968..22670018hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386018
hg196018
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560729
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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