A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831619



Internal ID22606554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14632078..14634549hg38UCSC Ensembl
chr2:14772202..14774673hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg382472
hg192472
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487758
Samples
Known GenesFAM84A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831619
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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