A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477308



Internal ID254894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:85471409..85478932hg38UCSC Ensembl
chr9:88086324..88093847hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg387524
hg197524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477308
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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