A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5998879



Internal ID21908222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8788820..8788941hg38UCSC Ensembl
chr4:8790546..8790667hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554716
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5998879
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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