A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989639



Internal ID21898982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38782633..38782707hg38UCSC Ensembl
chr2:39009775..39009849hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989639
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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