A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610714



Internal ID21559019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34418812..34418812hg38UCSC Ensembl
chr3:34460304..34460304hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119976
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610714
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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