A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981807



Internal ID21891150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:166647422..166654053hg38UCSC Ensembl
chr1:166616659..166623290hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg386632
hg196632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519192
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981807
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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