A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476622



Internal ID254229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122710365..122712949hg38UCSC Ensembl
chr9:125472644..125475228hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382585
hg192585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476622
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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