A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509481



Internal ID286132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119137545..119141658hg38UCSC Ensembl
chr11:119008255..119012368hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384114
hg194114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052231
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509481
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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