A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457922



Internal ID235957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74661042..74985754hg38UCSC Ensembl
chr6:75370758..75695470hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38324713
hg19324713
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv423n206
Supporting Variantsnssv16984634
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457922
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer