A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591036



Internal ID21539608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130092181..130092296hg38UCSC Ensembl
chr11:129962076..129962191hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17073516
SamplesHG00096
Known GenesAPLP2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591036
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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