A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621406



Internal ID21569711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146971441..146971441hg38UCSC Ensembl
chr4:147892593..147892593hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138128
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621406
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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