A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483078



Internal ID260521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86206496..86228810hg38UCSC Ensembl
chr9:88821411..88843725hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3822315
hg1922315
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738492
Samples
Known GenesC9orf153
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483078
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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