A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059606



Internal ID21968839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158105010..158105010hg38UCSC Ensembl
chr2:158961522..158961522hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535304
Samples
Known GenesUPP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059606
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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