A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091854



Internal ID22001087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73892487..73892487hg38UCSC Ensembl
chr11:73603532..73603532hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590779
Samples
Known GenesPAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091854
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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