A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529449



Internal ID305465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10111992..10112181hg38UCSC Ensembl
chr19:10222668..10222857hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721278
Samples
Known GenesP2RY11, PPAN-P2RY11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529449
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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