A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501630



Internal ID278523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113969193..113990314hg38UCSC Ensembl
chr11:113839915..113861036hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3821122
hg1921122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052503
Samples
Known GenesHTR3A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501630
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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