A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988239



Internal ID21897582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238296376..238296453hg38UCSC Ensembl
chr2:239205017..239205094hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988239
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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