A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989196



Internal ID21898539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:39848570..39872354hg38UCSC Ensembl
chr2:40075710..40099494hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3823785
hg1923785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989196
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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