A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879866



Internal ID22654836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50847896..50852862hg38UCSC Ensembl
chr19:51351152..51356118hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg384967
hg194967
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17477418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879866
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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