A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099035



Internal ID22008268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113935455..113935455hg38UCSC Ensembl
chr11:113806177..113806177hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17602854
Samples
Known GenesHTR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099035
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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