A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5984611



Internal ID21893954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:53468750..53504399hg38UCSC Ensembl
chr1:53934423..53970072hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3835650
hg1935650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521845
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5984611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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