A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5484312



Internal ID261726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4473864..4488225hg38UCSC Ensembl
chr10:4516056..4530417hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3814362
hg1914362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5484312
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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