A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995042



Internal ID21904385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98837542..98837720hg38UCSC Ensembl
chr3:98556386..98556564hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543419
Samples
Known GenesDCBLD2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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