A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484112



Internal ID261532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:10964933..10971241hg38UCSC Ensembl
chr9:10964933..10971241hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg386309
hg196309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021249
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484112
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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