A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998302



Internal ID21907645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66362990..66363256hg38UCSC Ensembl
chr4:67228708..67228974hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998302
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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