A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6099431



Internal ID22008664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113980730..113980730hg38UCSC Ensembl
chr11:113851452..113851452hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607586
Samples
Known GenesHTR3A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6099431
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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