A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889202



Internal ID22664217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131385289..131385883hg38UCSC Ensembl
chr3:131104133..131104727hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17402013
Samples
Known GenesNUDT16
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889202
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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