A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5614119



Internal ID21562424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108026325..108026325hg38UCSC Ensembl
chr3:107745172..107745172hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17125250
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5614119
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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