A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483813



Internal ID261240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:68610874..68611037hg38UCSC Ensembl
chr9:71225790..71225953hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483813
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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