A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980898



Internal ID21890241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121825482..121825995hg38UCSC Ensembl
chr1:121365848..121366361hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5980898
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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