A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066037



Internal ID21975270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171019123..171019123hg38UCSC Ensembl
chr3:170736912..170736912hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538789
Samples
Known GenesSLC2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066037
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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