A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17520114



Internal ID21844473
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 StatusS
Merged Variantsnsv5981777
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17520114
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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