A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459207



Internal ID237224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:149540391..149556381hg38UCSC Ensembl
chr6:149861527..149877517hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3815991
hg1915991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988988
Samples
Known GenesPPIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459207
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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