A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989596



Internal ID21898939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:59765024..59765115hg38UCSC Ensembl
chr2:59992159..59992250hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989596
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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