A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5619094



Internal ID21567399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38111184..38111184hg38UCSC Ensembl
chr2:38338326..38338326hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17113153
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5619094
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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