A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998022



Internal ID21907365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5811777..5811836hg38UCSC Ensembl
chr4:5813504..5813563hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554673
Samples
Known GenesEVC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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