A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5982261



Internal ID21891604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201456387..201468015hg38UCSC Ensembl
chr1:201425515..201437143hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3811629
hg1911629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518598
Samples
Known GenesPHLDA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5982261
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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