A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991207



Internal ID21900550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117024688..117026835hg38UCSC Ensembl
chr3:116743535..116745682hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg382148
hg192148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991207
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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