A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560368



Internal ID333377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:105993980..105994031hg38UCSC Ensembl
chr9:108756261..108756312hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg386016
hg196016
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560368
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