A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603862



Internal ID21552528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109228052..109228305hg38UCSC Ensembl
chr11:109098779..109099032hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38254
hg19254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072669
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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