A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092568



Internal ID22001801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92753798..92753798hg38UCSC Ensembl
chr11:92486964..92486964hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596876
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092568
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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