A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5828507



Internal ID22603442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16322327..16331091hg38UCSC Ensembl
chr1:16648822..16657586hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg388765
hg198765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454908
Samples
Known GenesFBXO42
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5828507
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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