A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766605



Internal ID20542465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126472989..126472989hg38UCSC Ensembl
chr11:126342884..126342884hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16296589
Samples
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766605
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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