A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889551



Internal ID22664570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90571563..90605841hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3834279
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889551
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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