A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17139298



Internal ID21470122
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 StatusS
Merged Variantsnsv5621070
Supporting Variants
SamplesHG03125
Known GenesSUMF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17139298
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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