A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753039



Internal ID20528899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17124424..17124424hg38UCSC Ensembl
chr11:17145971..17145971hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg382786
hg192786
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16260521
Samples
Known GenesPIK3C2A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753039
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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