A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5986998



Internal ID21896341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164626853..164630080hg38UCSC Ensembl
chr2:165483363..165486590hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg383228
hg193228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5986998
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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