A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980638



Internal ID21889981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106269518..106287334hg38UCSC Ensembl
chr1:106812140..106829956hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3817817
hg1917817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536675
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980638
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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