A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982828



Internal ID21892171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225470054..225499262hg38UCSC Ensembl
chr1:225657756..225686964hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3829209
hg1929209
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525247
Samples
Known GenesENAH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982828
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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