A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405093



Internal ID184438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110217165..110217216hg38UCSC Ensembl
chr6:110538368..110538419hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987947
Samples
Known GenesCDC40
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405093
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