A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296589



Internal ID20505807
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 StatusS
Merged Variantsnsv4766605
Supporting Variants
Samples
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296589
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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