A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484592



Internal ID262003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97129551..97132855hg38UCSC Ensembl
chr9:99891833..99895137hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg383305
hg193305
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027537
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484592
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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