A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5552604



Internal ID325935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113935455..113935455hg38UCSC Ensembl
chr11:113806177..113806177hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052499
Samples
Known GenesHTR3B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5552604
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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