A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5612245



Internal ID21560550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58185550..58185550hg38UCSC Ensembl
chr3:58171277..58171277hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17133704
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5612245
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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