A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488452



Internal ID265764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47138158..47141068hg38UCSC Ensembl
chr10:48598294..48601204hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382911
hg192911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488452
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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