A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521170



Internal ID297466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54220538..54336889hg38UCSC Ensembl
chr19:54724459..54848160hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38116352
hg19123702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17725506
Samples
Known GenesLILRA3, LILRA4, LILRA5, LILRA6, LILRB2, LILRB3, LILRB5, MIR4752
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521170
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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