A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870989



Internal ID22645927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32446676..32449165hg38UCSC Ensembl
chr19:32937582..32940071hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg382490
hg192490
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17474686
Samples
Known GenesDPY19L3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870989
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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