A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991454



Internal ID21900797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115150879..115150974hg38UCSC Ensembl
chr3:114869726..114869821hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545021
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991454
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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