A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5602099



Internal ID21550753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80654270..80654738hg38UCSC Ensembl
chr11:80365314..80365782hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38469
hg19469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17076253
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5602099
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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