A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073435



Internal ID21982668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171019734..171019734hg38UCSC Ensembl
chr3:170737523..170737523hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554498
Samples
Known GenesSLC2A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073435
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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