A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981096



Internal ID21890439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:144826063..144826703hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527169
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981096
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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