A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5611314



Internal ID21559619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170430707..170430707hg38UCSC Ensembl
chr3:170148495..170148495hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132543
SamplesNA12329
Known GenesCLDN11
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5611314
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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