A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5981009



Internal ID21890352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11916369..11916500hg38UCSC Ensembl
chr1:11976426..11976557hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528071
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5981009
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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