A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5991152



Internal ID21900495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:97665693..97665760hg38UCSC Ensembl
chr2:98282156..98282223hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518471
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5991152
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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