A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488533



Internal ID265843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:12460171..12612462hg38UCSC Ensembl
chr9:12460171..12612462hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38152292
hg19152292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17020459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488533
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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