A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662795



Internal ID21611100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62426177..62426177hg38UCSC Ensembl
chr11:62193649..62193649hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17075733
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662795
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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