A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5999486



Internal ID21908829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16624276..16624330hg38UCSC Ensembl
chr5:16624385..16624439hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17542956
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5999486
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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