A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996951



Internal ID21906294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26384894..26384979hg38UCSC Ensembl
chr4:26386516..26386601hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549983
Samples
Known GenesRBPJ
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996951
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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