A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610996



Internal ID21559301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194498482..194498482hg38UCSC Ensembl
chr3:194219211..194219211hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg383403
hg193403
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131670
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610996
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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