A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478477



Internal ID256031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87839787..87839837hg38UCSC Ensembl
chr10:89599544..89599594hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038395
Samples
Known GenesCFL1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478477
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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