A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5881103



Internal ID22656076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39100320..39106871hg38UCSC Ensembl
chr19:39590960..39597511hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg386552
hg196552
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475374
Samples
Known GenesPAPL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5881103
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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