A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502184



Internal ID279058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:125507201..125507523hg38UCSC Ensembl
chr11:125377097..125377419hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502184
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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