A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663146



Internal ID21611451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57593199..57593199hg38UCSC Ensembl
chr19:58104567..58104567hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17106490
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663146
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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