A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991841



Internal ID21901184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15454803..15457495hg38UCSC Ensembl
chr3:15496310..15499002hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg382693
hg192693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544382
Samples
Known GenesCOLQ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991841
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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