A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484549



Internal ID261959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66857387..66959387hg38UCSC Ensembl
chr9:40733454..40835454hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38102001
hg19102001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024175
Samples
Known GenesZNF658
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484549
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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