A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981777



Internal ID21891120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177982668..177988171hg38UCSC Ensembl
chr1:177951803..177957306hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg385504
hg195504
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520114
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981777
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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