A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420097



Internal ID199209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84132285..84132368hg38UCSC Ensembl
chr1:84597968..84598051hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905822
Samples
Known GenesPRKACB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420097
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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