A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516950



Internal ID293389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89315512..89315593hg38UCSC Ensembl
chr15:89858743..89858824hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704110
Samples
Known GenesFANCI
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516950
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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