A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999799



Internal ID21909142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:28596784..28596860hg38UCSC Ensembl
chr5:28596891..28596967hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555779
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999799
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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