A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980795



Internal ID21890138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12041255..12043987hg38UCSC Ensembl
chr1:12101312..12104044hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382733
hg192733
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523989
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980795
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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