A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5487909



Internal ID265231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23504396..23504477hg38UCSC Ensembl
chr9:23504394..23504475hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5487909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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