A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5618726



Internal ID21567031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84515386..84515386hg38UCSC Ensembl
chr1:84981069..84981069hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067042
SamplesNA12329
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5618726
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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