A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081289



Internal ID21990522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28100221..28100221hg38UCSC Ensembl
chr11:28121768..28121768hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588541
Samples
Known GenesKIF18A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081289
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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