A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496764



Internal ID273832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43540670..43540875hg38UCSC Ensembl
chr15:43832868..43833073hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702016
Samples
Known GenesPPIP5K1, RNU6-28P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496764
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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