A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619015



Internal ID21567320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120539995..120539995hg38UCSC Ensembl
chr3:120258842..120258842hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131260
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619015
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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