A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466874



Internal ID244701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:129546616..129574684hg38UCSC Ensembl
chr6:129867761..129895829hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg3828069
hg1928069
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16969381
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466874
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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