A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987630



Internal ID21896973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216513578..216515138hg38UCSC Ensembl
chr2:217378301..217379861hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg381561
hg191561
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519898
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987630
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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