A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619071



Internal ID21567376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186015086..186015086hg38UCSC Ensembl
chr3:185732875..185732875hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135276, nssv17124551
SamplesHG03125, HG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619071
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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