A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615788



Internal ID21564093
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 StatusM
Merged Variants
Supporting Variantsnssv17136901
SamplesNA20847
Known GenesNUP210
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615788
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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