A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753294



Internal ID20529154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133437606..133437606hg38UCSC Ensembl
chr11:133307501..133307501hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16283509
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753294
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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