A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660838



Internal ID21609143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106710081..106710081hg38UCSC Ensembl
chr11:106580807..106580807hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072441
SamplesHG00513
Known GenesGUCY1A2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660838
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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