A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5606029



Internal ID21554334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95003256..95003256hg38UCSC Ensembl
chr3:94722100..94722100hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg382274
hg192274
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123284
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5606029
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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