A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483221



Internal ID260661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:106392390..106392724hg38UCSC Ensembl
chr9:109154671..109155005hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025177
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483221
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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