A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5621070



Internal ID21569375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4363794..4363794hg38UCSC Ensembl
chr3:4405478..4405478hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139298
SamplesHG03125
Known GenesSUMF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5621070
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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