A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454589



Internal ID232687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62985986..63002616hg38UCSC Ensembl
chr6:63695891..63712521hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3816631
hg1916631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454589
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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