A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5884578



Internal ID22659561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1523049..1537465hg38UCSC Ensembl
chr19:1523048..1537464hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3814417
hg1914417
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473252
Samples
Known GenesPLK5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5884578
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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