A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067107



Internal ID21976340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:109469083..109469083hg38UCSC Ensembl
chr5:108804784..108804784hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067107
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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