A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5613178



Internal ID21561483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25058509..25058509hg38UCSC Ensembl
chr3:25100000..25100000hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381241
hg191241
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17119896
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5613178
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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