A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6091599



Internal ID22000832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69813638..69813638hg38UCSC Ensembl
chr11:69628406..69628406hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595323
Samples
Known GenesFGF3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6091599
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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