A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622191



Internal ID21570496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241456776..241456776hg38UCSC Ensembl
chr1:241620076..241620076hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17063656
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622191
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer