A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5983803



Internal ID21893146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32986547..32986835hg38UCSC Ensembl
chr1:33452148..33452436hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5983803
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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