A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136901



Internal ID21509452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13330458..13330458hg38UCSC Ensembl
chr3:13371958..13371958hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5615788
Supporting Variants
SamplesNA20847
Known GenesNUP210
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136901
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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