A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996269



Internal ID21905612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184032357..184032458hg38UCSC Ensembl
chr4:184953510..184953611hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996269
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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