A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432859



Internal ID21394861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54224129..54240124hg38UCSC Ensembl
chr19:54728001..54744000hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815996
hg1916000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750691
SamplesMDQ010
Known GenesLILRA6
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432859
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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