A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981658



Internal ID21891001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162104471..162394594hg38UCSC Ensembl
chr1:162074261..162364384hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38290124
hg19290124
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522472
Samples
Known GenesC1orf111, C1orf226, MIR4654, MIR556, NOS1AP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981658
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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